JPH0156061B2 - - Google Patents
Info
- Publication number
- JPH0156061B2 JPH0156061B2 JP2886986A JP2886986A JPH0156061B2 JP H0156061 B2 JPH0156061 B2 JP H0156061B2 JP 2886986 A JP2886986 A JP 2886986A JP 2886986 A JP2886986 A JP 2886986A JP H0156061 B2 JPH0156061 B2 JP H0156061B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- water
- hydrogen chloride
- parts
- hydrochloric acid
- 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.)
- Expired
Links
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 49
- 238000006243 chemical reaction Methods 0.000 claims description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 40
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 19
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 19
- 239000003960 organic solvent Substances 0.000 claims description 19
- 238000006722 reduction reaction Methods 0.000 claims description 16
- 150000002576 ketones Chemical class 0.000 claims description 14
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 5
- JIAARYAFYJHUJI-UHFFFAOYSA-L Zinc chloride Inorganic materials [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 3
- 239000012046 mixed solvent Substances 0.000 claims description 3
- 239000011592 zinc chloride Substances 0.000 claims description 3
- 238000010533 azeotropic distillation Methods 0.000 claims description 2
- 150000003997 cyclic ketones Chemical class 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 17
- 239000000047 product Substances 0.000 description 12
- 238000007086 side reaction Methods 0.000 description 8
- 238000009835 boiling Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N acetic acid anhydride Natural products CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UCPNHIPCCLLQGA-UHFFFAOYSA-N 2-hydroxycyclopentadecan-1-one Chemical compound OC1CCCCCCCCCCCCCC1=O UCPNHIPCCLLQGA-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- GXDHCNNESPLIKD-UHFFFAOYSA-N 2-methylhexane Chemical compound CCCCC(C)C GXDHCNNESPLIKD-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- 238000006657 acyloin condensation reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000000397 acetylating effect Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- -1 alcohol ester Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011027 product recovery Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2886986A JPS62190140A (ja) | 1986-02-14 | 1986-02-14 | 大環状ケトンの製造方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2886986A JPS62190140A (ja) | 1986-02-14 | 1986-02-14 | 大環状ケトンの製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62190140A JPS62190140A (ja) | 1987-08-20 |
JPH0156061B2 true JPH0156061B2 (US08124630-20120228-C00152.png) | 1989-11-28 |
Family
ID=12260383
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2886986A Granted JPS62190140A (ja) | 1986-02-14 | 1986-02-14 | 大環状ケトンの製造方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62190140A (US08124630-20120228-C00152.png) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63243049A (ja) * | 1987-03-31 | 1988-10-07 | Nippon Mining Co Ltd | 大環状ケトンの精製方法 |
-
1986
- 1986-02-14 JP JP2886986A patent/JPS62190140A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS62190140A (ja) | 1987-08-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Posner et al. | Short, simple, stereocontrolled, steroid synthesis:(.+-.)-11-oxoequilenin methyl ether and a new 9, 11-seco-13-ethyl steroid | |
Sommer et al. | Malonic Ester Syntheses with Organosilicon Compounds. New Silicon-containing Malonic Esters, Mono-and Dicarboxylic Acids, Barbituric Acids and a Disiloxanetetracarboxylic Acid1 | |
JPH0156061B2 (US08124630-20120228-C00152.png) | ||
US2748160A (en) | Process for preparing 2, 5-diacetoxysty-rene and intermediates therefor | |
Schreiber et al. | Stereochemical studies of simple cyclooctyl systems | |
JPS6156146A (ja) | 大環状ケトンの製造方法 | |
US2789988A (en) | Preparation of phthalic anhydride | |
JPS6230976B2 (US08124630-20120228-C00152.png) | ||
EP0230499B1 (en) | Process for preparing macrocyclic ketones | |
CH640496A5 (fr) | Procede pour la preparation de beta-damascenone. | |
Watanabe et al. | A New Preparative Method of 1, 6-Diketones from Fatty Acids and Vinylmagnesium Chloride | |
JP4100007B2 (ja) | シクロペンテノロン類の精製方法 | |
JPH08119924A (ja) | 3,7−ジメチル−2,6−オクタジエンニトリルの異性化方法 | |
JP2720054B2 (ja) | トリメリット酸エステル無水物の製造方法 | |
JP4100003B2 (ja) | シクロペンテノロン類の精製方法 | |
JPH045009B2 (US08124630-20120228-C00152.png) | ||
JPH0155259B2 (US08124630-20120228-C00152.png) | ||
JPS6366302B2 (US08124630-20120228-C00152.png) | ||
JPH0156059B2 (US08124630-20120228-C00152.png) | ||
JPH02165A (ja) | 1‐クロトノイル‐2,6,6‐トリメチルシクロヘキサー1,3‐ジエンの製造法 | |
JPH04346959A (ja) | α,β−不飽和アセタール類の高濃度溶液の精製方法 | |
JPH11322659A (ja) | 不飽和アルデヒドの製造方法 | |
JPH0535134B2 (US08124630-20120228-C00152.png) | ||
JP3312811B2 (ja) | トランス−1,4−シクロヘキサンジメタノールジアルキルスルホネートの精製方法 | |
JP4009763B2 (ja) | ベンジルアセテートの精製方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313111 |
|
R371 | Transfer withdrawn |
Free format text: JAPANESE INTERMEDIATE CODE: R371 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313111 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
EXPY | Cancellation because of completion of term |