Butyryl chloride → HCID 70240726, 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])[CH2:20][CH2:21][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])[CH2:20][CH2:21][CH3:22]

Participants

Reactant 2

HCID 8855Butyryl chloride

HCID 10514571HCID 10514571, compound

Product 1

HCID 70240726HCID 70240726, 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 butyryl chloride.

Sources & evidence

ORD record: ord-c6377497629f4f7983981390a471f03d
Source dataset: uspto-grants-2001_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06255339B1

Reaction notes

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