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Hydrochloric Acid → 3-Bromo-4-chlorobenzaldehyde

HRID 1275839
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HRID 1275839 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][C:13]=1[Cl:14])[C:5](N(OC)C)=[O:6].[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[NH4+].Cl>O1CCCC1>[Br:1][C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][C:13]=1[Cl:14])[CH:5]=[O:6]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 25517Ammonium ChlorideHCID 21226445Aluminium lithium hydrideHCID 22117812HCID 22117812, 화합물

생성물 1

HCID 140498093-Bromo-4-chlorobenzaldehyde수율 80.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회
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실험 절차

A solution of 10.7 g of 3-bromo-4-chloro-N-methoxy-N-methylbenzamide in 100 ml of anhydrous tetrahydrofuran was added dropwise to 43 ml of a 1M solution of lithium aluminium hydride in tetrahydrofuran at below 5° C., and stirred for 1 hour. 100 ml of saturated ammonium chloride solution was then added cautiously followed by 100 ml of a 1M solution of hydrochloric acid and the mixture was extracted twice with 400 ml of diethyl ether. The combined organic extracts were dried over anhydrous sodium sulphate and concentrated under reduced pressure to give 6.8 g of 3-bromo-4-chlorobenzaldehyde as a pale yellow solid.

후처리

  1. extractionthe mixture was extracted twice with 400 ml of diethyl ether
  2. dry with materialThe combined organic extracts were dried over anhydrous sodium sulphate
  3. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-814a2a4b25a74e638e6b5a855f76014b
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06162918

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