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Ethanol → 2-Cyano-3-hydroxymethylthiophene

HRID 1952840
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HRID 1952840 반응식
[BH4-].[Na+].[C:3]([C:5]1[S:6][CH:7]=[C:8](C=O)C=1)#[N:4].[CH2:12]([OH:14])[CH3:13]>>[C:3]([C:5]1[S:6][CH:7]=[CH:8][C:13]=1[CH2:12][OH:14])#[N:4]
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참가 물질

4

반응물 3

HCID 702EthanolHCID 4311764Sodium borohydrideHCID 122800084-Formylthiophene-2-carbonitrile

생성물 1

HCID 218664902-Cyano-3-hydroxymethylthiophene수율 91.5%

실험 절차

3.47 g (91.8 mmol) of sodium borohydride were added in portions to a suspension of 12.6 g (91.8 mmol) of 2-cyano-4-formylthiophene in 200 ml of ethanol, and the reaction mixture was stirred at room temperature for 2 h, during which it slowly formed a clear solution. The residue after concentration under reduced pressure was taken up in ethyl acetate and washed successively with saturated brine, 5% strength citric acid and saturated brine, and the organic phase was dried with sodium sulfate and concentrated under reduced pressure to result in 11.7 g of almost pure product (yield 91.5%).

후처리

  1. customslowly formed a clear solution
  2. concentrationThe residue after concentration under reduced pressure
  3. washwashed successively with saturated brine, 5% strength citric acid and saturated brine
  4. dry with materialthe organic phase was dried with sodium sulfate
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-0c59f81e6c3b413f916c26efaee5a75f
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06114358

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