Benzoyl chloride → HCID 70240269, compound

Reaction equation

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

Participants

Reactant 2

HCID 7412Benzoyl chloride

HCID 10514571HCID 10514571, compound

Product 1

HCID 70240269HCID 70240269, compound

Procedure

The title compound was prepared in the same manner as in Example B2, except that the compound prepared in Example B1 was reacted with benzoyl chloride.

Sources & evidence

ORD record: ord-cf99e5861a6940f68a40b833e2782208
Source dataset: uspto-grants-2001_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06255339B1

Reaction notes

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