JPS6056147B2 - ３−ブロムフタリドの製法 - Google Patents
３−ブロムフタリドの製法Info
- Publication number
- JPS6056147B2 JPS6056147B2 JP13775977A JP13775977A JPS6056147B2 JP S6056147 B2 JPS6056147 B2 JP S6056147B2 JP 13775977 A JP13775977 A JP 13775977A JP 13775977 A JP13775977 A JP 13775977A JP S6056147 B2 JPS6056147 B2 JP S6056147B2
- Authority
- JP
- Japan
- Prior art keywords
- bromphthalide
- hydrogen bromide
- reaction
- chlorophthalide
- bromide
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- CLMSHAWYULIVFQ-UHFFFAOYSA-N 3-bromo-3h-2-benzofuran-1-one Chemical compound C1=CC=C2C(Br)OC(=O)C2=C1 CLMSHAWYULIVFQ-UHFFFAOYSA-N 0.000 claims description 15
- GHZPDRVHYHFILK-UHFFFAOYSA-N 3-chloro-3h-2-benzofuran-1-one Chemical compound C1=CC=C2C(Cl)OC(=O)C2=C1 GHZPDRVHYHFILK-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 4
- 150000004820 halides Chemical class 0.000 claims description 3
- 230000000737 periodic effect Effects 0.000 claims description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 31
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 10
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical group 0.000 description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000010626 work up procedure Methods 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 230000004584 weight gain Effects 0.000 description 2
- 235000019786 weight gain Nutrition 0.000 description 2
- -1 α,β-monounsaturated cyclic chloroketones Chemical class 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910001513 alkali metal bromide Inorganic materials 0.000 description 1
- 229910001616 alkaline earth metal bromide Inorganic materials 0.000 description 1
- 150000001348 alkyl chlorides Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005633 phthalidyl group Chemical group 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/87—Benzo [c] furans; Hydrogenated benzo [c] furans
- C07D307/88—Benzo [c] furans; Hydrogenated benzo [c] furans with one oxygen atom directly attached in position 1 or 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2652299.6 | 1976-11-17 | ||
| DE19762652299 DE2652299B2 (de) | 1976-11-17 | 1976-11-17 | Verfahren zur Herstellung von 3-Bromphthalid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5363372A JPS5363372A (en) | 1978-06-06 |
| JPS6056147B2 true JPS6056147B2 (ja) | 1985-12-09 |
Family
ID=5993339
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13775977A Expired JPS6056147B2 (ja) | 1976-11-17 | 1977-11-16 | ３−ブロムフタリドの製法 |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS6056147B2 (cs) |
| BE (1) | BE860901A (cs) |
| CH (1) | CH630622A5 (cs) |
| DE (1) | DE2652299B2 (cs) |
| DK (1) | DK143132C (cs) |
| ES (1) | ES464174A1 (cs) |
| FR (1) | FR2371440A1 (cs) |
| GB (1) | GB1537815A (cs) |
| IT (1) | IT1112096B (cs) |
| NL (1) | NL7712620A (cs) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2934822A1 (de) * | 1979-08-29 | 1981-03-19 | Dynamit Nobel Ag, 5210 Troisdorf | Verfahren zur herstellung von 3-bromphthalid |
| CN116041295B (zh) * | 2023-03-31 | 2023-06-06 | 寿光祥铭化工有限公司 | 一种3-溴苯酞的制备方法 |
-
1976
- 1976-11-17 DE DE19762652299 patent/DE2652299B2/de active Granted
-
1977
- 1977-11-15 GB GB4754277A patent/GB1537815A/en not_active Expired
- 1977-11-15 IT IT5181877A patent/IT1112096B/it active
- 1977-11-16 NL NL7712620A patent/NL7712620A/xx not_active Application Discontinuation
- 1977-11-16 JP JP13775977A patent/JPS6056147B2/ja not_active Expired
- 1977-11-16 ES ES464174A patent/ES464174A1/es not_active Expired
- 1977-11-16 CH CH1401277A patent/CH630622A5/de not_active IP Right Cessation
- 1977-11-16 DK DK507977A patent/DK143132C/da not_active IP Right Cessation
- 1977-11-16 FR FR7734473A patent/FR2371440A1/fr active Granted
- 1977-11-17 BE BE182675A patent/BE860901A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DK507977A (da) | 1978-05-18 |
| IT1112096B (it) | 1986-01-13 |
| DK143132B (da) | 1981-06-29 |
| DK143132C (da) | 1981-11-23 |
| FR2371440B1 (cs) | 1982-07-09 |
| FR2371440A1 (fr) | 1978-06-16 |
| CH630622A5 (en) | 1982-06-30 |
| NL7712620A (nl) | 1978-05-19 |
| DE2652299C3 (cs) | 1979-04-26 |
| DE2652299A1 (de) | 1978-05-18 |
| BE860901A (fr) | 1978-03-16 |
| DE2652299B2 (de) | 1978-08-31 |
| JPS5363372A (en) | 1978-06-06 |
| GB1537815A (en) | 1979-01-04 |
| ES464174A1 (es) | 1978-09-01 |
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