CN104478719A - 一种4-甲氧基乙酰乙酸甲酯的制备方法 - Google Patents
一种4-甲氧基乙酰乙酸甲酯的制备方法 Download PDFInfo
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- CN104478719A CN104478719A CN201510033422.3A CN201510033422A CN104478719A CN 104478719 A CN104478719 A CN 104478719A CN 201510033422 A CN201510033422 A CN 201510033422A CN 104478719 A CN104478719 A CN 104478719A
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- Prior art keywords
- methyl acetoacetate
- temperature
- kettle
- methoxyl group
- add
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- 238000002360 preparation method Methods 0.000 title claims abstract description 13
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 51
- 238000006243 chemical reaction Methods 0.000 claims abstract description 50
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims abstract description 45
- 239000002904 solvent Substances 0.000 claims abstract description 44
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims abstract description 30
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 28
- 229910000104 sodium hydride Inorganic materials 0.000 claims abstract description 25
- 239000012312 sodium hydride Substances 0.000 claims abstract description 24
- 238000000199 molecular distillation Methods 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 14
- 238000001514 detection method Methods 0.000 claims abstract description 14
- 229910052751 metal Inorganic materials 0.000 claims abstract description 13
- 239000002184 metal Substances 0.000 claims abstract description 13
- WRQNANDWMGAFTP-UHFFFAOYSA-N Methylacetoacetic acid Chemical compound COC(=O)CC(C)=O WRQNANDWMGAFTP-UHFFFAOYSA-N 0.000 claims description 28
- VWVZFHRDLPHBEG-UHFFFAOYSA-N 1-(chloromethyl)-4-methylsulfanylbenzene Chemical group CSC1=CC=C(CCl)C=C1 VWVZFHRDLPHBEG-UHFFFAOYSA-N 0.000 claims description 21
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 14
- 238000013517 stratification Methods 0.000 claims description 13
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 claims description 11
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 3
- 239000012279 sodium borohydride Substances 0.000 claims description 3
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 claims description 3
- 230000033228 biological regulation Effects 0.000 claims description 2
- 239000011259 mixed solution Substances 0.000 claims description 2
- 238000010792 warming Methods 0.000 claims description 2
- 238000003756 stirring Methods 0.000 abstract description 45
- 239000007788 liquid Substances 0.000 abstract description 14
- 238000004821 distillation Methods 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 239000012535 impurity Substances 0.000 abstract description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 3
- 238000001035 drying Methods 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- HFLMYYLFSNEOOT-UHFFFAOYSA-N methyl 4-chloro-3-oxobutanoate Chemical compound COC(=O)CC(=O)CCl HFLMYYLFSNEOOT-UHFFFAOYSA-N 0.000 abstract 1
- 230000000630 rising effect Effects 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 132
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 22
- 239000012141 concentrate Substances 0.000 description 22
- 239000003921 oil Substances 0.000 description 22
- 239000000243 solution Substances 0.000 description 22
- 238000000034 method Methods 0.000 description 14
- 239000002480 mineral oil Substances 0.000 description 13
- 235000010446 mineral oil Nutrition 0.000 description 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 11
- 239000008346 aqueous phase Substances 0.000 description 11
- 229910052786 argon Inorganic materials 0.000 description 11
- 238000001816 cooling Methods 0.000 description 11
- 238000004128 high performance liquid chromatography Methods 0.000 description 11
- 238000002156 mixing Methods 0.000 description 11
- 239000012074 organic phase Substances 0.000 description 11
- 238000002390 rotary evaporation Methods 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- 238000010025 steaming Methods 0.000 description 11
- 239000000725 suspension Substances 0.000 description 11
- 238000005406 washing Methods 0.000 description 11
- RHWKPHLQXYSBKR-BMIGLBTASA-N dolutegravir Chemical compound C([C@@H]1OCC[C@H](N1C(=O)C1=C(O)C2=O)C)N1C=C2C(=O)NCC1=CC=C(F)C=C1F RHWKPHLQXYSBKR-BMIGLBTASA-N 0.000 description 6
- 229960002542 dolutegravir Drugs 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 208000030507 AIDS Diseases 0.000 description 1
- 229940124321 AIDS medicine Drugs 0.000 description 1
- 229940099797 HIV integrase inhibitor Drugs 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003084 hiv integrase inhibitor Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229940124524 integrase inhibitor Drugs 0.000 description 1
- 239000002850 integrase inhibitor Substances 0.000 description 1
- YWOITFUKFOYODT-UHFFFAOYSA-N methanol;sodium Chemical compound [Na].OC YWOITFUKFOYODT-UHFFFAOYSA-N 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 229960004742 raltegravir Drugs 0.000 description 1
- CZFFBEXEKNGXKS-UHFFFAOYSA-N raltegravir Chemical compound O1C(C)=NN=C1C(=O)NC(C)(C)C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C CZFFBEXEKNGXKS-UHFFFAOYSA-N 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229940014075 tivicay Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/31—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
- C07C67/52—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
- C07C67/54—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Polyethers (AREA)
- Lubricants (AREA)
- Cosmetics (AREA)
Abstract
Description
Claims (4)
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CN201510033422.3A CN104478719B (zh) | 2015-01-23 | 2015-01-23 | 一种4-甲氧基乙酰乙酸甲酯的制备方法 |
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CN201510033422.3A CN104478719B (zh) | 2015-01-23 | 2015-01-23 | 一种4-甲氧基乙酰乙酸甲酯的制备方法 |
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CN104478719A true CN104478719A (zh) | 2015-04-01 |
CN104478719B CN104478719B (zh) | 2016-08-10 |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105418420A (zh) * | 2015-12-04 | 2016-03-23 | 河南师范大学 | 一种4-甲氧基乙酰乙酸甲酯的合成方法 |
CN105481694A (zh) * | 2015-12-04 | 2016-04-13 | 河南师范大学 | 一种4-甲氧基乙酰乙酸乙酯的合成方法 |
CN113831242A (zh) * | 2021-10-11 | 2021-12-24 | 瑞孚信江苏药业股份有限公司 | 一种4-甲氧基乙酰乙酸甲酯的制备方法 |
CN114213249A (zh) * | 2021-12-31 | 2022-03-22 | 瑞孚信江苏药业股份有限公司 | 一种度鲁特韦中间体的合成方法 |
CN114349635A (zh) * | 2021-12-31 | 2022-04-15 | 瑞孚信江苏药业股份有限公司 | 一种度鲁特韦核心中间体的合成方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB942664A (en) * | 1960-04-06 | 1963-11-27 | Director | Improved methods of producing dimethyl ª -ketoadipate and dimethyl ª -methyl ª -ketoadipate |
US4564696A (en) * | 1981-10-01 | 1986-01-14 | Lonza Ltd. | Process for the production of 4-alkoxyacetoacetic acid esters |
US6403804B1 (en) * | 1998-12-07 | 2002-06-11 | Takasago International Corporation | Process for preparing optically active oxazolidinone derivative |
CN1962683A (zh) * | 2006-12-18 | 2007-05-16 | 张文芳 | 聚乙二醇修饰的甾醇共聚物及其应用 |
-
2015
- 2015-01-23 CN CN201510033422.3A patent/CN104478719B/zh active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB942664A (en) * | 1960-04-06 | 1963-11-27 | Director | Improved methods of producing dimethyl ª -ketoadipate and dimethyl ª -methyl ª -ketoadipate |
US4564696A (en) * | 1981-10-01 | 1986-01-14 | Lonza Ltd. | Process for the production of 4-alkoxyacetoacetic acid esters |
US6403804B1 (en) * | 1998-12-07 | 2002-06-11 | Takasago International Corporation | Process for preparing optically active oxazolidinone derivative |
CN1962683A (zh) * | 2006-12-18 | 2007-05-16 | 张文芳 | 聚乙二醇修饰的甾醇共聚物及其应用 |
Non-Patent Citations (1)
Title |
---|
朱利平等: "Williamson 法合成两亲性聚醚砜酮-聚乙二醇接枝共聚物", 《高分子学报》 * |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105418420A (zh) * | 2015-12-04 | 2016-03-23 | 河南师范大学 | 一种4-甲氧基乙酰乙酸甲酯的合成方法 |
CN105481694A (zh) * | 2015-12-04 | 2016-04-13 | 河南师范大学 | 一种4-甲氧基乙酰乙酸乙酯的合成方法 |
CN107311861A (zh) * | 2015-12-04 | 2017-11-03 | 朱海燕 | 一种4‑甲氧基乙酰乙酸乙酯及其合成方法 |
CN107311861B (zh) * | 2015-12-04 | 2020-04-21 | 高邮市华宝颜料有限公司 | 一种4-甲氧基乙酰乙酸乙酯及其合成方法 |
CN113831242A (zh) * | 2021-10-11 | 2021-12-24 | 瑞孚信江苏药业股份有限公司 | 一种4-甲氧基乙酰乙酸甲酯的制备方法 |
CN114213249A (zh) * | 2021-12-31 | 2022-03-22 | 瑞孚信江苏药业股份有限公司 | 一种度鲁特韦中间体的合成方法 |
CN114349635A (zh) * | 2021-12-31 | 2022-04-15 | 瑞孚信江苏药业股份有限公司 | 一种度鲁特韦核心中间体的合成方法 |
CN114349635B (zh) * | 2021-12-31 | 2023-09-01 | 瑞孚信江苏药业股份有限公司 | 一种度鲁特韦核心中间体的合成方法 |
CN114213249B (zh) * | 2021-12-31 | 2023-09-01 | 瑞孚信江苏药业股份有限公司 | 一种度鲁特韦中间体的合成方法 |
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CN104478719B (zh) | 2016-08-10 |
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Effective date of registration: 20170704 Address after: 362216 Fujian city of Quanzhou province Jinjiang city Luoshan Street Building No. 1208 Aetna world city Patentee after: Quanzhou Intelligent Technology Co., Ltd. Address before: 453007 Xinxiang East Road, Makino District, Henan, No. 46 Patentee before: Henan Normal University |
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CB03 | Change of inventor or designer information |
Inventor after: Mao Longfei Inventor after: Chen Jiarui Inventor after: Li Wei Inventor after: Kou Lidong Inventor after: Jiang Yuqin Inventor after: Dong Wenpei Inventor after: Mao Along Inventor after: Chen Xiaohua Inventor after: Wan Zhong Inventor after: Li Debing Inventor before: Mao Longfei Inventor before: Li Wei Inventor before: Kou Lidong Inventor before: Jiang Yuqin Inventor before: Dong Wenpei Inventor before: Mao Along Inventor before: Chen Xiaohua Inventor before: Wan Zhong |
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Effective date of registration: 20170710 Address after: 528400 No. 63 Hongshan Road, Xiaolan Town, Guangdong, Zhongshan Patentee after: Guangdong Xiangshan Pharmaceutical Co., Ltd. Address before: 362216 Fujian city of Quanzhou province Jinjiang city Luoshan Street Building No. 1208 Aetna world city Patentee before: Quanzhou Intelligent Technology Co., Ltd. |
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Denomination of invention: A preparation method of methyl 4-methoxyacetoacetate Effective date of registration: 20200728 Granted publication date: 20160810 Pledgee: Haikou United Rural Commercial Bank Limited by Share Ltd. Pledgor: GUANGDONG XIANGSHANTANG PHARMACEUTICAL Co.,Ltd. Registration number: Y2020980004444 |
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Date of cancellation: 20210901 Granted publication date: 20160810 Pledgee: Haikou United Rural Commercial Bank Limited by Share Ltd. Pledgor: GUANGDONG XIANGSHANTANG PHARMACEUTICAL Co.,Ltd. Registration number: Y2020980004444 |
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Denomination of invention: A preparation method of methyl 4-methoxyacetoacetate Effective date of registration: 20210903 Granted publication date: 20160810 Pledgee: Haikou United Rural Commercial Bank Limited by Share Ltd. Pledgor: GUANGDONG XIANGSHANTANG PHARMACEUTICAL Co.,Ltd. Registration number: Y2021440000279 |
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