Propionyl chloride → HCID 70237597, compound

HRID 1383621Notes

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:22])[CH2:20][CH3:21]>>[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:22])[CH2:20][CH3:21]

Participants

Reactant 2

HCID 62324Propionyl chloride

HCID 10514571HCID 10514571, compound

Product 1

HCID 70237597HCID 70237597, compound

Procedure

The title compound was prepared in the same manner as in Example B2, except that the compound prepared in Example B1 (2) Method B was reacted with propionyl chloride.

Sources & evidence

ORD record: ord-f1ef5956931a4634b41c83ba0d966407
Source dataset: uspto-grants-2001_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06255339B1

Reaction notes

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