Benzyl Bromide → HCID 20531466, compound

HRID 1732320Notes

Reaction equation

[CH2:1]([C:3]1([CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:12][C:11]2[C:6](=[C:7]([OH:15])[CH:8]=[C:9]([CH:13]=[O:14])[CH:10]=2)[C:5](=[O:16])[CH2:4]1)[CH3:2].[CH2:24](Br)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[CH2:1]([C:3]1([CH2:17][C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:12][C:11]2[C:6](=[C:7]([O:15][CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[CH:8]=[C:9]([CH:13]=[O:14])[CH:10]=2)[C:5](=[O:16])[CH2:4]1)[CH3:2]

Participants

Reactant 2

HCID 7498Benzyl Bromide

HCID 20531444HCID 20531444, compound

Product 1

HCID 20531466HCID 20531466, compound

Procedure

The product of Example 35 is benzylated with benzyl bromide as described in Example 15.

Sources & evidence

ORD record: ord-499a20469a4d4687bf2504faee6b2a1b
Source dataset: uspto-grants-1980_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04237133

Reaction notes

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