Isobutyryl chloride → HCID 67622567, 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:23])[CH:20]([CH3:22])[CH3:21]>>[CH3:21][CH:20]([CH3:22])[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:23]

Participants

Reactant 2

HCID 62325Isobutyryl chloride

HCID 10514571HCID 10514571, compound

Product 1

HCID 67622567HCID 67622567, 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 isobutyryl chloride.

Sources & evidence

ORD record: ord-62bae5a6c1df4c9080e4d431c3960a3f
Source dataset: uspto-grants-2001_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06255339B1

Reaction notes

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