CN105461516A - 一种l-薄荷醇的合成工艺 - Google Patents
一种l-薄荷醇的合成工艺 Download PDFInfo
- Publication number
- CN105461516A CN105461516A CN201510809332.9A CN201510809332A CN105461516A CN 105461516 A CN105461516 A CN 105461516A CN 201510809332 A CN201510809332 A CN 201510809332A CN 105461516 A CN105461516 A CN 105461516A
- Authority
- CN
- China
- Prior art keywords
- menthol
- phenylformic acid
- menthyl ester
- rectifying
- reaction
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 title claims abstract description 191
- 238000000034 method Methods 0.000 title claims abstract description 66
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims abstract description 203
- 229940041616 menthol Drugs 0.000 claims abstract description 76
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 claims abstract description 44
- 230000032050 esterification Effects 0.000 claims abstract description 40
- 238000005886 esterification reaction Methods 0.000 claims abstract description 40
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 32
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 32
- 238000002425 crystallisation Methods 0.000 claims abstract description 23
- 230000008025 crystallization Effects 0.000 claims abstract description 23
- 239000005844 Thymol Substances 0.000 claims abstract description 22
- 229960000790 thymol Drugs 0.000 claims abstract description 22
- NOOLISFMXDJSKH-AEJSXWLSSA-N (+)-menthol Chemical compound CC(C)[C@H]1CC[C@H](C)C[C@@H]1O NOOLISFMXDJSKH-AEJSXWLSSA-N 0.000 claims abstract description 21
- 238000006317 isomerization reaction Methods 0.000 claims abstract description 20
- 239000002994 raw material Substances 0.000 claims abstract description 13
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 130
- 150000002148 esters Chemical class 0.000 claims description 118
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 81
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 75
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 claims description 72
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 52
- 238000006243 chemical reaction Methods 0.000 claims description 51
- 239000000047 product Substances 0.000 claims description 42
- 229940095102 methyl benzoate Drugs 0.000 claims description 33
- 229910052739 hydrogen Inorganic materials 0.000 claims description 23
- 239000001257 hydrogen Substances 0.000 claims description 23
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 19
- 229910000564 Raney nickel Inorganic materials 0.000 claims description 19
- 238000004821 distillation Methods 0.000 claims description 19
- 239000013078 crystal Substances 0.000 claims description 16
- 238000005984 hydrogenation reaction Methods 0.000 claims description 16
- 238000001953 recrystallisation Methods 0.000 claims description 14
- 238000010992 reflux Methods 0.000 claims description 12
- 239000000706 filtrate Substances 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 10
- 238000004845 hydriding Methods 0.000 claims description 9
- 238000011084 recovery Methods 0.000 claims description 9
- 238000010583 slow cooling Methods 0.000 claims description 9
- 238000007710 freezing Methods 0.000 claims description 8
- 230000008014 freezing Effects 0.000 claims description 8
- 230000001186 cumulative effect Effects 0.000 claims description 6
- -1 d in a kettle. Chemical compound 0.000 claims description 6
- 238000000605 extraction Methods 0.000 claims description 6
- 238000009413 insulation Methods 0.000 claims description 6
- 230000003287 optical effect Effects 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 239000012295 chemical reaction liquid Substances 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 238000005194 fractionation Methods 0.000 claims description 3
- 239000012452 mother liquor Substances 0.000 claims description 3
- 238000000967 suction filtration Methods 0.000 claims description 3
- NFLGAXVYCFJBMK-IUCAKERBSA-N (-)-isomenthone Chemical compound CC(C)[C@@H]1CC[C@H](C)CC1=O NFLGAXVYCFJBMK-IUCAKERBSA-N 0.000 claims description 2
- YSTPAHQEHQSRJD-SECBINFHSA-N (-)-piperitone Chemical compound CC(C)[C@H]1CCC(C)=CC1=O YSTPAHQEHQSRJD-SECBINFHSA-N 0.000 claims description 2
- 229930006950 (-)-piperitone Natural products 0.000 claims description 2
- 238000000746 purification Methods 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 4
- 239000000126 substance Substances 0.000 abstract description 7
- 238000011031 large-scale manufacturing process Methods 0.000 abstract description 3
- 238000002360 preparation method Methods 0.000 abstract description 3
- 239000002351 wastewater Substances 0.000 abstract description 3
- 230000009286 beneficial effect Effects 0.000 abstract description 2
- 230000002194 synthesizing effect Effects 0.000 abstract 3
- 238000010924 continuous production Methods 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 230000007613 environmental effect Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 235000013599 spices Nutrition 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 description 12
- 238000005809 transesterification reaction Methods 0.000 description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 239000008241 heterogeneous mixture Substances 0.000 description 6
- 102000004190 Enzymes Human genes 0.000 description 5
- 108090000790 Enzymes Proteins 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000006555 catalytic reaction Methods 0.000 description 3
- WTEVQBCEXWBHNA-JXMROGBWSA-N citral A Natural products CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 2
- 241000134874 Geraniales Species 0.000 description 2
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 2
- 230000002255 enzymatic effect Effects 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- ZYTMANIQRDEHIO-KXUCPTDWSA-N isopulegol Chemical compound C[C@@H]1CC[C@@H](C(C)=C)[C@H](O)C1 ZYTMANIQRDEHIO-KXUCPTDWSA-N 0.000 description 2
- VNDYJBBGRKZCSX-UHFFFAOYSA-L zinc bromide Chemical compound Br[Zn]Br VNDYJBBGRKZCSX-UHFFFAOYSA-L 0.000 description 2
- 239000001871 (1R,2R,5S)-5-methyl-2-prop-1-en-2-ylcyclohexan-1-ol Substances 0.000 description 1
- NOOLISFMXDJSKH-IVZWLZJFSA-N (1r,2r,5s)-5-methyl-2-propan-2-ylcyclohexan-1-ol Chemical compound CC(C)[C@H]1CC[C@H](C)C[C@H]1O NOOLISFMXDJSKH-IVZWLZJFSA-N 0.000 description 1
- YSTPAHQEHQSRJD-UHFFFAOYSA-N 3-Carvomenthenone Chemical compound CC(C)C1CCC(C)=CC1=O YSTPAHQEHQSRJD-UHFFFAOYSA-N 0.000 description 1
- 241000985905 Candidatus Phytoplasma solani Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000208125 Nicotiana Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000011914 asymmetric synthesis Methods 0.000 description 1
- KMPWYEUPVWOPIM-UHFFFAOYSA-N cinchonidine Natural products C1=CC=C2C(C(C3N4CCC(C(C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-UHFFFAOYSA-N 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229940095045 isopulegol Drugs 0.000 description 1
- 229960004873 levomenthol Drugs 0.000 description 1
- AHNJTQYTRPXLLG-UHFFFAOYSA-N lithium;diethylazanide Chemical compound [Li+].CC[N-]CC AHNJTQYTRPXLLG-UHFFFAOYSA-N 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- ZYTMANIQRDEHIO-UHFFFAOYSA-N neo-Isopulegol Natural products CC1CCC(C(C)=C)C(O)C1 ZYTMANIQRDEHIO-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229930006968 piperitone Natural products 0.000 description 1
- 238000010956 selective crystallization Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940102001 zinc bromide Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/17—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds
- C07C29/19—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds in six-membered aromatic rings
- C07C29/20—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds in six-membered aromatic rings in a non-condensed rings substituted with hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/76—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
- C07C29/78—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by condensation or crystallisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Description
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510809332.9A CN105461516B8 (zh) | 2015-11-20 | 2015-11-20 | 一种l-薄荷醇的合成工艺 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510809332.9A CN105461516B8 (zh) | 2015-11-20 | 2015-11-20 | 一种l-薄荷醇的合成工艺 |
Publications (3)
Publication Number | Publication Date |
---|---|
CN105461516A true CN105461516A (zh) | 2016-04-06 |
CN105461516B CN105461516B (zh) | 2017-12-29 |
CN105461516B8 CN105461516B8 (zh) | 2018-06-08 |
Family
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Family Applications (1)
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CN201510809332.9A Active CN105461516B8 (zh) | 2015-11-20 | 2015-11-20 | 一种l-薄荷醇的合成工艺 |
Country Status (1)
Country | Link |
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CN (1) | CN105461516B8 (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110354909A (zh) * | 2019-07-18 | 2019-10-22 | 万华化学集团股份有限公司 | 一种制备l-薄荷醇的催化剂体系及其制备方法和应用 |
CN111892483A (zh) * | 2020-08-03 | 2020-11-06 | 万香科技股份有限公司 | 一种拆分d,l-薄荷醇的方法 |
CN117547471A (zh) * | 2024-01-11 | 2024-02-13 | 万华化学集团股份有限公司 | 一种具有改善的凉感透发性的l薄荷醇组合物及其应用 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB341654A (en) * | 1929-01-28 | 1931-01-22 | Rheinische Kampfer Fabrik Ges | A process for preparing pure inactive menthol |
US3943181A (en) * | 1971-02-27 | 1976-03-09 | Haarmann & Reimer Gesellschaft Mit Beschrankter Haftung | Separating optically pure d-l-isomers of menthol, neomenthol and isomenthol |
CN103910607A (zh) * | 2014-04-03 | 2014-07-09 | 上海应用技术学院 | 一种利用柱前衍生高效液相色谱法拆分dl-薄荷醇的方法 |
CN104888794A (zh) * | 2015-05-21 | 2015-09-09 | 浙江新和成股份有限公司 | 金属复合物催化剂、其制备方法以及在制备d,l-薄荷醇中的应用 |
-
2015
- 2015-11-20 CN CN201510809332.9A patent/CN105461516B8/zh active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB341654A (en) * | 1929-01-28 | 1931-01-22 | Rheinische Kampfer Fabrik Ges | A process for preparing pure inactive menthol |
US3943181A (en) * | 1971-02-27 | 1976-03-09 | Haarmann & Reimer Gesellschaft Mit Beschrankter Haftung | Separating optically pure d-l-isomers of menthol, neomenthol and isomenthol |
CN103910607A (zh) * | 2014-04-03 | 2014-07-09 | 上海应用技术学院 | 一种利用柱前衍生高效液相色谱法拆分dl-薄荷醇的方法 |
CN104888794A (zh) * | 2015-05-21 | 2015-09-09 | 浙江新和成股份有限公司 | 金属复合物催化剂、其制备方法以及在制备d,l-薄荷醇中的应用 |
Non-Patent Citations (1)
Title |
---|
王铃: "l-薄荷醇合成工艺研究", 《中国优秀硕士学位论文全文数据库 工程科技Ⅰ辑 (月刊 )》 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110354909A (zh) * | 2019-07-18 | 2019-10-22 | 万华化学集团股份有限公司 | 一种制备l-薄荷醇的催化剂体系及其制备方法和应用 |
CN110354909B (zh) * | 2019-07-18 | 2022-01-07 | 万华化学集团股份有限公司 | 一种制备l-薄荷醇的催化剂体系及其制备方法和应用 |
CN111892483A (zh) * | 2020-08-03 | 2020-11-06 | 万香科技股份有限公司 | 一种拆分d,l-薄荷醇的方法 |
CN111892483B (zh) * | 2020-08-03 | 2022-11-04 | 万香科技股份有限公司 | 一种拆分d,l-薄荷醇的方法 |
CN117547471A (zh) * | 2024-01-11 | 2024-02-13 | 万华化学集团股份有限公司 | 一种具有改善的凉感透发性的l薄荷醇组合物及其应用 |
CN117547471B (zh) * | 2024-01-11 | 2024-05-03 | 万华化学集团股份有限公司 | 一种具有改善的凉感透发性的l薄荷醇组合物及其应用 |
Also Published As
Publication number | Publication date |
---|---|
CN105461516B8 (zh) | 2018-06-08 |
CN105461516B (zh) | 2017-12-29 |
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Inventor after: Jie Fengxian Inventor after: Zhang Qizhong Inventor after: Hao Zongxian Inventor after: Bai Yang Inventor after: Zhang Xinya Inventor after: Gui Yue Inventor after: Tang Mingsheng Inventor before: Jie Fengxian Inventor before: Zhang Qizhong Inventor before: Hao Zongxian Inventor before: Bai Yang |
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Correction item: Fifth inventor Correct: Zhang Yaxin False: Zhang Xinya Number: 52-02 Page: The title page Volume: 33 Correction item: Fifth inventor Correct: Zhang Yaxin False: Zhang Xinya False: Zhang Xinya Number: 52-02 Volume: 33 Volume: 33 |
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Address after: 233300 No.36 Kaiyuan Avenue, mohekou Industrial Park, Huaishang District, Bengbu City, Anhui Province Patentee after: Anhui Haihua Technology Co., Ltd. Address before: 233000 Anhui province Bengbu Kaiyuan Avenue estuary Industrial Park Huaishang District No. 34 Mo Patentee before: Anhui Haihua Chemical Technology Co., Ltd. |
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Address after: 233000 No.36, Kaiyuan Avenue, mohekou Industrial Park, Huaishang District, Bengbu City, Anhui Province Patentee after: Anhui Haihua Technology Group Co.,Ltd. Address before: 233300 No.36, Kaiyuan Avenue, mohekou Industrial Park, Huaishang District, Bengbu City, Anhui Province Patentee before: Anhui Haihua Technology Co.,Ltd. |