Hydrochloric Acid → 4-Chloro-5-(4-chlorophenoxy)-2-nitrobenzoic Acid

HRID 231900

反応式

HRID 231900 の反応式
[H-].[Na+].[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.[Cl:11][C:12]1[C:20](Cl)=[CH:19][C:15]([C:16]([OH:18])=[O:17])=[C:14]([N+:22]([O-:24])=[O:23])[CH:13]=1.Cl>COCCOCCOC>[Cl:11][C:12]1[C:20]([O:10][C:7]2[CH:8]=[CH:9][C:4]([Cl:3])=[CH:5][CH:6]=2)=[CH:19][C:15]([C:16]([OH:18])=[O:17])=[C:14]([N+:22]([O-:24])=[O:23])[CH:13]=1

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 46844-ChlorophenolHCID 24758Sodium hydrideHCID 5836424,5-Dichloro-2-nitrobenzoic acid

生成物 1

HCID 142334244-Chloro-5-(4-chlorophenoxy)-2-nitrobenzoic Acid

試薬・触媒・溶媒 1

HCID 8150Diglyme溶媒3 回

反応条件

温度
10 °C

実験手順

To 30 ml of dry diglyme under a nitrogen atmosphere was added 0.960 g (0.02 mol) cf sodium hydride dispersion in mineral oil (50%). The solution was cooled to 10° C. and 1.28 g (0.01M) 4-chlorophenol in 15 ml of dry diglyme was added dropwise while maintaining the temperature at 10° C. This was followed by the dropwise addition of 2.36 g (0.01 mol) of 4,5-dichloro-2-nitrobenzoic acid in 15 ml of dry diglyme. The reaction mixture was then heated to 153° C. (oil bath) for 1 hour and 45 minutes. The reaction mixture was cooled to room temperature and poured into an ice/water mixture. The pH was then adjusted to 1.5 with 6N hydrochloric acid. The solution was extracted with ethyl acetate, and the organic layer dried over anhydrous magnesium sulfate. The solvent was removed and the crude solid triturated with hexane, followed by recrystallization from carbon tetrachloride to give the title compound: yield 1.65 g (50%) m.p. 160°-162° C.

後処理

  1. temperaturewhile maintaining the temperature at 10° C
  2. temperatureThe reaction mixture was then heated to 153° C. (oil bath) for 1 hour
  3. custom45 minutes
  4. temperatureThe reaction mixture was cooled to room temperature
  5. extractionThe solution was extracted with ethyl acetate
  6. dry with materialthe organic layer dried over anhydrous magnesium sulfate
  7. customThe solvent was removed
  8. customthe crude solid triturated with hexane
  9. customfollowed by recrystallization from carbon tetrachloride

出典と根拠

ORDレコード
ord-81bc965b63994068b5b85b7bcbce073c
出典データセット
uspto-grants-1989_07
特許番号
US04849518

関連ノート

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