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Lithium borohydride → (3-Benzyloxy-4-iodophenyl)methanol

HRID 250869
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인쇄 미리보기

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HRID 250869 반응식
[BH4-].[Li+].[CH2:3]([O:10][C:11]1[CH:12]=[C:13]([CH:18]=[CH:19][C:20]=1[I:21])[C:14](OC)=[O:15])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>O1CCCC1>[CH2:3]([O:10][C:11]1[CH:12]=[C:13]([CH2:14][OH:15])[CH:18]=[CH:19][C:20]=1[I:21])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4148881Lithium borohydrideHCID 57443321Methyl 3-(benzyloxy)-4-iodobenzoate

생성물 1

HCID 45140291(3-Benzyloxy-4-iodophenyl)methanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

1.18 g (54 mmol, 3 eq) of lithium borohydride are added to a solution of 6.9 g of methyl 3-benzyloxy-4-iodobenzoate in 30 ml of tetrahydrofuran. The reaction medium is heated at 60° C. for 12 hours and then hydrolyzed with ammonium chloride solution and extracted with ethyl acetate. The organic phases are combined and the solvents are evaporated off. 6.5 g of (3-benzyloxy-4-iodophenyl)methanol in oil form are used in the following reaction without further purification.

후처리

  1. extractionhydrolyzed with ammonium chloride solution and extracted with ethyl acetate
  2. customthe solvents are evaporated off
  3. custom6.5 g of (3-benzyloxy-4-iodophenyl)methanol in oil form are used in the following reaction without further purification

출처 및 근거

ORD 기록
ord-729da5f1eed4487da047b3d0a10cfb8a
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863332B2

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