Octanoyl chloride → HCID 136393676, compound

HRID 652790Notes

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:33])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]>>[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:33])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]

Participants

Reactant 2

HCID 8124Octanoyl chloride

HCID 136393672HCID 136393672, compound

Product 1

HCID 136393676HCID 136393676, compound

Procedure

3,5-di-t-butyl-4-hydroxybenzophenone oxime and octanoyl chloride were treated in the same was as in Example 3 to give 3,5-di-t-butyl-4-hydroxybenzophenone O-octanoyloxime.

Sources & evidence

ORD record: ord-16868f2a0f1a4b52908c39b569eea72d
Source dataset: uspto-grants-1987_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04673692

Reaction notes

Loading…