JPS6225653B2 - - Google Patents
Info
- Publication number
- JPS6225653B2 JPS6225653B2 JP15858282A JP15858282A JPS6225653B2 JP S6225653 B2 JPS6225653 B2 JP S6225653B2 JP 15858282 A JP15858282 A JP 15858282A JP 15858282 A JP15858282 A JP 15858282A JP S6225653 B2 JPS6225653 B2 JP S6225653B2
- Authority
- JP
- Japan
- Prior art keywords
- acetic acid
- butyl acetate
- acetate
- polyhydric alcohol
- butyl
- 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
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 75
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 21
- 150000005846 sugar alcohols Polymers 0.000 claims description 10
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 8
- 238000004821 distillation Methods 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 235000013773 glyceryl triacetate Nutrition 0.000 description 4
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 4
- 229960002622 triacetin Drugs 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 description 3
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- AOGQPLXWSUTHQB-UHFFFAOYSA-N hexyl acetate Chemical compound CCCCCCOC(C)=O AOGQPLXWSUTHQB-UHFFFAOYSA-N 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- UYAAVKFHBMJOJZ-UHFFFAOYSA-N diimidazo[1,3-b:1',3'-e]pyrazine-5,10-dione Chemical compound O=C1C2=CN=CN2C(=O)C2=CN=CN12 UYAAVKFHBMJOJZ-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229940116423 propylene glycol diacetate Drugs 0.000 description 1
- -1 softeners Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical class CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15858282A JPS5948444A (ja) | 1982-09-10 | 1982-09-10 | 多価アルコ−ル酢酸エステルの精製方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15858282A JPS5948444A (ja) | 1982-09-10 | 1982-09-10 | 多価アルコ−ル酢酸エステルの精製方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5948444A JPS5948444A (ja) | 1984-03-19 |
JPS6225653B2 true JPS6225653B2 (enrdf_load_stackoverflow) | 1987-06-04 |
Family
ID=15674834
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15858282A Granted JPS5948444A (ja) | 1982-09-10 | 1982-09-10 | 多価アルコ−ル酢酸エステルの精製方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5948444A (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0438293U (enrdf_load_stackoverflow) * | 1990-07-30 | 1992-03-31 |
-
1982
- 1982-09-10 JP JP15858282A patent/JPS5948444A/ja active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0438293U (enrdf_load_stackoverflow) * | 1990-07-30 | 1992-03-31 |
Also Published As
Publication number | Publication date |
---|---|
JPS5948444A (ja) | 1984-03-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR20100036303A (ko) | (메트)아크릴레이트의 제조 방법 | |
KR20100036302A (ko) | 에틸렌 글리콜 디메타크릴레이트의 제조 방법 | |
JPH04330063A (ja) | アルキルイミダゾリドン(メタ)アクリレートの製造方法 | |
ATE318255T1 (de) | Verfahren zur herstellung von estern | |
MY117817A (en) | Purification process for removal of impurities in acetic acid-ethylene reactions | |
ATE543793T1 (de) | Verfahren zur herstellung von benzoesäureestern | |
KR101522743B1 (ko) | 부탄디올 디메타크릴레이트의 제조 방법 | |
JPH04230240A (ja) | モノエチレン不飽和カルボン酸エステルの製造法 | |
KR20120056844A (ko) | 미정제 글리세롤의 정제 방법 | |
JP3672818B2 (ja) | (メタ)アクリル酸エステルの精製方法 | |
US4983761A (en) | Process for the preparation of high-boiling acrylates and methacrylates | |
ATE234805T1 (de) | Verfahren zur veresterung in einem chromatographischen reaktor | |
JPS6225653B2 (enrdf_load_stackoverflow) | ||
US3991100A (en) | Process for making esters of dibasic acids from acid by-products | |
CZ369196A3 (en) | Esterification of (meth)acrylic acid with alkanol | |
JPH11193262A (ja) | ヒドロキシアルキルモノ(メタ)アクリレートの製造方法 | |
JP5697832B2 (ja) | ホールセル−生体内変換からの反応溶液の後処理 | |
JP2002363132A (ja) | 2,2,4−トリメチル−1,3−ペンタンジオールジイソブチレートの製造方法 | |
JP2001288147A (ja) | メタクリル酸メチルの精製方法 | |
US6967257B1 (en) | Method of purifying lactic acid esters | |
JP3880128B2 (ja) | アクリル酸の回収方法 | |
JPH02152945A (ja) | 2−(4−ヒドロキシフェノキシ)プロピオン酸エステルの精製法 | |
JP2002234863A (ja) | (メタ)アクリル酸エステルの精製方法および(メタ)アクリル酸エステル | |
US5618971A (en) | Separation of a mono(meth)acrylate of a C4 -C6 alkanediol from an aqueous solution containing a mono(methacrylate) of a C4 -C6 alkanediol and the said C4 -C6 alkanediol | |
JPS647064B2 (enrdf_load_stackoverflow) |