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

HRID 250869
Notes
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Reaction equation

HRID 250869 reaction equation
[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
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
60 °C

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-729da5f1eed4487da047b3d0a10cfb8a
Source dataset
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07863332B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes