KR890012930A - 고순도 테트라클로로-1,4-벤조퀴논의 제조방법 - Google Patents
고순도 테트라클로로-1,4-벤조퀴논의 제조방법 Download PDFInfo
- Publication number
- KR890012930A KR890012930A KR1019880001049A KR880001049A KR890012930A KR 890012930 A KR890012930 A KR 890012930A KR 1019880001049 A KR1019880001049 A KR 1019880001049A KR 880001049 A KR880001049 A KR 880001049A KR 890012930 A KR890012930 A KR 890012930A
- Authority
- KR
- South Korea
- Prior art keywords
- molar amount
- hydrochloric acid
- benzoquinone
- hydrogen peroxide
- hydroquinone
- Prior art date
Links
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 title claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 10
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 8
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims 8
- 239000000725 suspension Substances 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- KSFNQTZBTVALRV-UHFFFAOYSA-N 2,3,5-trichlorocyclohexa-2,5-diene-1,4-dione Chemical compound ClC1=CC(=O)C(Cl)=C(Cl)C1=O KSFNQTZBTVALRV-UHFFFAOYSA-N 0.000 claims 1
- AYNPIRVEWMUJDE-UHFFFAOYSA-N 2,5-dichlorohydroquinone Chemical compound OC1=CC(Cl)=C(O)C=C1Cl AYNPIRVEWMUJDE-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C50/00—Quinones
- C07C50/24—Quinones containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C46/00—Preparation of quinones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/62—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C46/00—Preparation of quinones
- C07C46/02—Preparation of quinones by oxidation giving rise to quinoid structures
- C07C46/06—Preparation of quinones by oxidation giving rise to quinoid structures of at least one hydroxy group on a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (3)
- 3.8 내지 4.2배 몰량의 30 내지 37% 염산 및 1.9 내지 2.1 배몰량의 50 내지 35% 과산화수소를 5 내지 50℃에서, 적어도 12배 몰량의 30 내지 37% 염산중의 하이드로퀴논 1몰에 작용시킨 다음, 필수적으로 2.5-디클로로하이드로퀴논을 함유하는 생성된 현탁액을 45 내지 55℃까지 가열하고, 이 현탁액에, 각 경우에 사용된 하이드로퀴논을 기준하여, 3.8 내지 4.2배 몰량의 30 내지 37% 염산 및, 1.9 내지 2.1배 몰량의 50 내지 35% 과산화수소를 50 내지 95℃에서 작용시킨 후, 최종적으로 필수적으로 트리클로로-1,4-벤조퀴논으로 이루어진 현탁액에, 각 경우에 사용된 하이드로퀴논을 기준하여, 1.9 내지 2.1배 몰량의 상기 농도 범위의 염산 및 0.95 내지 1.05배 몰량의 상기 농도 범위의 과산화수소를 95 내지 115℃에서 염소가 방출되지 않도록 충분하게 서서히 가함을 특징으로 하여, 과산화수소 및 염산을 하이드로퀴논에 작용시킴으로써 고순도의 테트라클로로-1,4-벤조퀴논을 제조하는 방법.
- 제1항에 있어서, 산 및 염소에 안정한 계면활성제의 존재하에서 수행하는 방법.
- 제1항 또는 2항에 있어서, 2급 알칸설포네이트의 존재하에서 수행하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE87-3703567 | 1987-02-06 | ||
DEP3703567.3 | 1987-02-06 | ||
DE19873703567 DE3703567A1 (de) | 1987-02-06 | 1987-02-06 | Verfahren zur herstellung von tetrachlor-1,4-benzochinon hoher reinheit |
Publications (2)
Publication Number | Publication Date |
---|---|
KR890012930A true KR890012930A (ko) | 1989-09-20 |
KR960001705B1 KR960001705B1 (ko) | 1996-02-03 |
Family
ID=6320345
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019880001049A KR960001705B1 (ko) | 1987-02-06 | 1988-02-05 | 고순도 테트라클로로-1,4-벤조퀴논의 제조방법 |
Country Status (9)
Country | Link |
---|---|
US (1) | US5151532A (ko) |
EP (1) | EP0278377B1 (ko) |
JP (1) | JPH0832653B2 (ko) |
KR (1) | KR960001705B1 (ko) |
BR (1) | BR8800476A (ko) |
CA (1) | CA1313879C (ko) |
DE (2) | DE3703567A1 (ko) |
ES (1) | ES2036606T3 (ko) |
IN (1) | IN166876B (ko) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5329027A (en) * | 1992-11-24 | 1994-07-12 | Grupo Cydsa, S.A. De C.V. | Oxidative dehalogenation process for the production of perchlorinated quinones |
DE4336323C1 (de) * | 1993-10-25 | 1995-03-09 | Hoechst Ag | Verfahren zur Herstellung von Tetrachlor- 1,4-benzochinon |
DE4405929C1 (de) * | 1994-02-24 | 1995-03-09 | Hoechst Ag | Verfahren zur Herstellung von Tetrachlor-1,4-benzochinon |
US7458257B2 (en) * | 2005-12-19 | 2008-12-02 | Schlumberger Technology Corporation | Downhole measurement of formation characteristics while drilling |
CN106866399B (zh) * | 2017-03-03 | 2020-05-22 | 南通书创药业科技有限公司 | 四氯苯醌及其制备方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2722537A (en) * | 1953-01-23 | 1955-11-01 | Monsanto Chemicals | Production of chloranil |
DE2645114A1 (de) * | 1976-10-06 | 1978-04-13 | Peter Prof Dr Boldt | Verfahren zur halogenierung und halogenierenden oxydation aromatischer verbindungen |
DE2933119C2 (de) * | 1979-08-16 | 1982-06-24 | Chemische Fabrik Kalk GmbH, 5000 Köln | Verfahren zur Herstellung von Bromanil |
-
1987
- 1987-02-06 DE DE19873703567 patent/DE3703567A1/de not_active Withdrawn
-
1988
- 1988-01-18 IN IN43/CAL/88A patent/IN166876B/en unknown
- 1988-02-03 EP EP88101533A patent/EP0278377B1/de not_active Expired - Lifetime
- 1988-02-03 ES ES198888101533T patent/ES2036606T3/es not_active Expired - Lifetime
- 1988-02-03 DE DE8888101533T patent/DE3869804D1/de not_active Expired - Fee Related
- 1988-02-05 JP JP63024074A patent/JPH0832653B2/ja not_active Expired - Lifetime
- 1988-02-05 CA CA000558259A patent/CA1313879C/en not_active Expired - Fee Related
- 1988-02-05 KR KR1019880001049A patent/KR960001705B1/ko not_active IP Right Cessation
- 1988-02-06 BR BR8800476A patent/BR8800476A/pt active Search and Examination
-
1991
- 1991-06-27 US US07/724,499 patent/US5151532A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US5151532A (en) | 1992-09-29 |
BR8800476A (pt) | 1988-09-20 |
EP0278377A3 (en) | 1989-04-26 |
DE3703567A1 (de) | 1988-08-18 |
IN166876B (ko) | 1990-07-28 |
EP0278377A2 (de) | 1988-08-17 |
JPH0832653B2 (ja) | 1996-03-29 |
DE3869804D1 (de) | 1992-05-14 |
CA1313879C (en) | 1993-02-23 |
EP0278377B1 (de) | 1992-04-08 |
KR960001705B1 (ko) | 1996-02-03 |
ES2036606T3 (es) | 1993-06-01 |
JPS63196539A (ja) | 1988-08-15 |
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