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Tetrabutylammonium borohydride → (3-o-Tolylbenzo[b]thiophen-2-yl)methanol

HRID 242862
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인쇄 미리보기

반응식

HRID 242862 반응식
[BH4-].C([N+](CCCC)(CCCC)CCCC)CCC.[C:19]1([CH3:36])[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[C:25]1[C:26]2[CH:35]=[CH:34][CH:33]=[CH:32][C:27]=2[S:28][C:29]=1[CH:30]=[O:31]>C1COCC1>[C:19]1([CH3:36])[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[C:25]1[C:26]2[CH:35]=[CH:34][CH:33]=[CH:32][C:27]=2[S:28][C:29]=1[CH2:30][OH:31]
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참가 물질

4

반응물 2

HCID 169536Tetrabutylammonium borohydrideHCID 866688743-o-Tolylbenzo[b]thiophene-2-carbaldehyde

생성물 1

HCID 68157058(3-o-Tolylbenzo[b]thiophen-2-yl)methanol수율 82.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Tetrabutylammonium borohydride (nBu4NBH4) (800 mg, 3.10 mmol) was added at RT to a solution of 3-o-tolylbenzo[b]thiophene-2-carbaldehyde (2.07 mmol) in THF (10 mL) and IMS (1 mL) and the mixture was stirred at RT for 1 h. The reaction mixture was then quenched by addition of MeOH and volatiles were removed under reduced pressure. The resulting residues was purified by column chromatography (Si—PCC, gradient 0-30% EtOAc in cyclohexane) affording the title compound as an oil (432 mg, 82% over 2 steps). LCMS: RT 3.74 min [M-OH]+ 237.1.

후처리

  1. customThe reaction mixture was then quenched by addition of MeOH and volatiles
  2. customwere removed under reduced pressure
  3. customThe resulting residues was purified by column chromatography (Si—PCC, gradient 0-30% EtOAc in cyclohexane)

출처 및 근거

ORD 기록
ord-6383a86f30a842bfaf1b4c0067a4d71f
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653089B2

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