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Lithium borohydride → 2-Hydroxy-4-(hydroxymethyl)benzonitrile

HRID 379029
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HRID 379029 반응식
[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7](OC)=[O:8])=[CH:5][C:4]=1[OH:13])#[N:2].[Li+].[BH4-]>C1COCC1>[OH:13][C:4]1[CH:5]=[C:6]([CH2:7][OH:8])[CH:11]=[CH:12][C:3]=1[C:1]#[N:2]
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참가 물질

4

반응물 2

HCID 4148881Lithium borohydrideHCID 16641129Methyl 4-cyano-3-hydroxybenzoate

생성물 1

HCID 216969742-Hydroxy-4-(hydroxymethyl)benzonitrile

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Methyl 4-cyano-3-hydroxybenzoate, as described in Example 4, Step C, (0.50 g, 2.82 mmol) was dissolved in dry THF (30 mL), treated with LiBH4 (2.0M solution in THF) (5.64 mL, 11.28 mmol) and heated at reflux overnight. The reaction mixture was concentrated, then partitioned between EtOAc (50 mL) and 1N HCl (50 mL). Next, the aqueous layer was extracted with additional EtOAc (2×50 mL), the organic layers were combined, washed with brine, and dried (MgSO4). The title compounds was obtained by filtering and concentrating to dryness.

후처리

  1. temperatureheated
  2. temperatureat reflux overnight
  3. concentrationThe reaction mixture was concentrated
  4. custompartitioned between EtOAc (50 mL) and 1N HCl (50 mL)
  5. extractionNext, the aqueous layer was extracted with additional EtOAc (2×50 mL)
  6. washwashed with brine
  7. dry with materialdried (MgSO4)

출처 및 근거

ORD 기록
ord-cfc0a830161845479db49df7ee137ff5
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06297239B1

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