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Sodium borohydride → HCID 12875271, 화합물

HRID 1764585
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HRID 1764585 반응식
[Br:1][C:2]1[C:3]([CH3:10])=[C:4]([CH:8]=[O:9])[S:5][C:6]=1[CH3:7].[BH4-].[Na+]>C(O)C>[Br:1][C:2]1[C:3]([CH3:10])=[C:4]([CH2:8][OH:9])[S:5][C:6]=1[CH3:7]
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 128752694-Bromo-3,5-dimethylthiophene-2-carbaldehyde

생성물 1

HCID 12875271HCID 12875271, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

11.8 G. of 4-bromo-3,5-dimethylthiophene-2-carboxaldehyde was dissolved in 250 ml. of dry ethanol and stirred at 20° C. 0.52 G. of sodium borohydride was added and the resulting solution was stirred for 30 minutes, then poured into ice water and extracted with ethyl ether. The combined ether extracts were washed with a solution of 5% sodium carbonate and a saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. Crystallization from cold hexane yielded 4-bromo-3,5-dimethyl-2-hydroxymethylthiophene, m.p. 85°-90° C.

후처리

  1. extractionextracted with ethyl ether
  2. washThe combined ether extracts were washed with a solution of 5% sodium carbonate
  3. dry with materiala saturated sodium chloride solution, dried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated
  6. customCrystallization from cold hexane

출처 및 근거

ORD 기록
ord-e746f5ea0df94f59a639aab0f59c7f67
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04116975

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