RU2002112475A - METHOD FOR PRODUCING ARYLALKYL ETHERS - Google Patents
METHOD FOR PRODUCING ARYLALKYL ETHERSInfo
- Publication number
- RU2002112475A RU2002112475A RU2002112475/04A RU2002112475A RU2002112475A RU 2002112475 A RU2002112475 A RU 2002112475A RU 2002112475/04 A RU2002112475/04 A RU 2002112475/04A RU 2002112475 A RU2002112475 A RU 2002112475A RU 2002112475 A RU2002112475 A RU 2002112475A
- Authority
- RU
- Russia
- Prior art keywords
- alcohol
- catalyst
- hydroxyaromatic compound
- above items
- hydroxyaromatic
- Prior art date
Links
- 150000002170 ethers Chemical class 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 5
- 239000003054 catalyst Substances 0.000 claims 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 3
- YCIMNLLNPGFGHC-UHFFFAOYSA-N Catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N P-Cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 claims 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N Resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N benzohydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N n-butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N t-BuOH Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-Naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 claims 1
- -1 arylalkyl ethers Chemical class 0.000 claims 1
- 235000019445 benzyl alcohol Nutrition 0.000 claims 1
- 229950011260 betanaphthol Drugs 0.000 claims 1
- 238000004821 distillation Methods 0.000 claims 1
- 239000008240 homogeneous mixture Substances 0.000 claims 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N n-pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 239000002244 precipitate Substances 0.000 claims 1
- 239000000047 product Substances 0.000 claims 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propanol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
Claims (6)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19949319A DE19949319A1 (en) | 1999-10-13 | 1999-10-13 | Process for the preparation of aryl alkyl ethers |
DE19949319.7 | 1999-10-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2002112475A true RU2002112475A (en) | 2003-12-10 |
RU2245869C2 RU2245869C2 (en) | 2005-02-10 |
Family
ID=7925469
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2002112475/04A RU2245869C2 (en) | 1999-10-13 | 2000-10-04 | Arylalkyl ether manufacturing method |
Country Status (15)
Country | Link |
---|---|
US (1) | US6624334B1 (en) |
EP (1) | EP1224157B1 (en) |
JP (1) | JP2003511430A (en) |
KR (1) | KR100716077B1 (en) |
CN (1) | CN1263719C (en) |
AT (1) | ATE285391T1 (en) |
AU (1) | AU7661600A (en) |
CA (1) | CA2388218A1 (en) |
DE (2) | DE19949319A1 (en) |
IL (2) | IL148761A0 (en) |
MX (1) | MXPA02003739A (en) |
PL (1) | PL200685B1 (en) |
RU (1) | RU2245869C2 (en) |
WO (1) | WO2001027060A1 (en) |
ZA (1) | ZA200202146B (en) |
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WO2009110510A1 (en) | 2008-03-06 | 2009-09-11 | 萬有製薬株式会社 | Alkylaminopyridine derivative |
EP2272841A1 (en) | 2008-03-28 | 2011-01-12 | Banyu Pharmaceutical Co., Ltd. | Diarylmethylamide derivative having antagonistic activity on melanin-concentrating hormone receptor |
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CN108002988B (en) * | 2017-11-24 | 2020-12-15 | 西安近代化学研究所 | Preparation method of 1, 2-di (2- (2, 6-dimethoxyphenoxy) ethoxy) ethane |
WO2019119363A1 (en) * | 2017-12-21 | 2019-06-27 | 中国科学院大连化学物理研究所 | Method for producing mixed ether from mixed phenol and methol by gas phase etherification |
CN108569957B (en) * | 2018-05-04 | 2021-08-10 | 南京师范大学 | Device and method for extracting 2-naphthyl methyl ether from 2-naphthol, methanol, 2-naphthyl methyl ether and p-toluenesulfonic acid and recovering components |
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CN109879728B (en) * | 2019-02-01 | 2022-04-19 | 宝鸡文理学院 | Method for synthesizing anisole by catalyzing phenol and methanol |
CN109809970B (en) * | 2019-02-01 | 2022-05-06 | 宝鸡文理学院 | Method for producing anisole by catalyzing phenol and methanol |
CN109879727B (en) * | 2019-02-01 | 2022-04-19 | 宝鸡文理学院 | Method for synthesizing anisole from phenol and methanol |
CN109879730B (en) * | 2019-02-01 | 2022-04-19 | 宝鸡文理学院 | Method for producing anisole from phenol and methanol |
CN116082125A (en) * | 2023-03-17 | 2023-05-09 | 山东兴文工业技术研究院有限公司 | Method for preparing beta-anisole by dynamic tubular reactor |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3911022A (en) * | 1973-06-04 | 1975-10-07 | Eastman Kodak Co | Etherification of phenolic compounds |
US4487975A (en) * | 1980-03-31 | 1984-12-11 | Rhone-Poulenc Industries | Etherification of phenols |
FR2513633A1 (en) * | 1981-09-29 | 1983-04-01 | Rhone Poulenc Spec Chim | PHENOLS ETHERIFICATION PROCESS |
FR2488883A1 (en) * | 1980-08-25 | 1982-02-26 | Rhone Poulenc Ind | PHENOLS ETHERIFICATION PROCESS |
-
1999
- 1999-10-13 DE DE19949319A patent/DE19949319A1/en not_active Withdrawn
-
2000
- 2000-10-04 CA CA002388218A patent/CA2388218A1/en not_active Abandoned
- 2000-10-04 IL IL14876100A patent/IL148761A0/en active IP Right Grant
- 2000-10-04 US US10/110,011 patent/US6624334B1/en not_active Expired - Fee Related
- 2000-10-04 RU RU2002112475/04A patent/RU2245869C2/en not_active IP Right Cessation
- 2000-10-04 AT AT00966108T patent/ATE285391T1/en not_active IP Right Cessation
- 2000-10-04 PL PL354121A patent/PL200685B1/en not_active IP Right Cessation
- 2000-10-04 KR KR1020027004681A patent/KR100716077B1/en not_active IP Right Cessation
- 2000-10-04 DE DE50009060T patent/DE50009060D1/en not_active Expired - Fee Related
- 2000-10-04 JP JP2001530082A patent/JP2003511430A/en active Pending
- 2000-10-04 CN CNB008137161A patent/CN1263719C/en not_active Expired - Fee Related
- 2000-10-04 MX MXPA02003739A patent/MXPA02003739A/en active IP Right Grant
- 2000-10-04 EP EP00966108A patent/EP1224157B1/en not_active Expired - Lifetime
- 2000-10-04 WO PCT/EP2000/009699 patent/WO2001027060A1/en active IP Right Grant
- 2000-10-04 AU AU76616/00A patent/AU7661600A/en not_active Abandoned
-
2002
- 2002-03-15 ZA ZA200202146A patent/ZA200202146B/en unknown
- 2002-03-19 IL IL148761A patent/IL148761A/en not_active IP Right Cessation
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