Sodium borohydride → 3-(4-Bromophenoxy)benzyl alcohol

HRID 483731

Reaction equation

[BH4-].[Na+].[Br:3][C:4]1[CH:18]=[CH:17][C:7]([O:8][C:9]2[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=2)[CH:12]=[O:13])=[CH:6][CH:5]=1>>[Br:3][C:4]1[CH:18]=[CH:17][C:7]([O:8][C:9]2[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=2)[CH2:12][OH:13])=[CH:6][CH:5]=1

Participants

Reactant 2

HCID 4311764Sodium borohydride

HCID 128743633-(4-Bromophenoxy)benzaldehyde

Product 1

HCID 145170543-(4-Bromophenoxy)benzyl alcohol

Procedure

This compound was prepared by a standard sodium borohydride reduction from 3-(4-bromophenoxy)benzaldehyde.

Sources & evidence

ORD record: ord-5d88e6814d6a4d47ac94531daad1db6d
Source dataset: uspto-grants-1993_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05225607

Linked notes

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