Propionyl chloride → HCID 136393674, compound

HRID 652788Notes

Reaction equation

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

Participants

Reactant 2

HCID 62324Propionyl chloride

HCID 136393672HCID 136393672, compound

Product 1

HCID 136393674HCID 136393674, compound

Procedure

3,5-di-t-butyl-4-hydroxybenzophenone oxime and propionyl chloride were treated in the same way as in Example 3 to obtain 3,5-di-t-butyl-4-hydroxybenzophenone O-propionyloxime.

Sources & evidence

ORD record: ord-682b31f11f334c6da4087470e9ae3d1e
Source dataset: uspto-grants-1987_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04673692

Reaction notes

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