Propionyl chloride → HCID 20185249, compound

HRID 2309415Notes

Reaction equation

[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH2:10][CH2:11][CH3:12])[C:5]=1[O:13][CH3:14])[CH2:2][CH3:3].[C:15](Cl)(=[O:18])[CH2:16][CH3:17]>>[C:15]([C:8]1[CH:9]=[C:4]([CH2:1][CH2:2][CH3:3])[C:5]([O:13][CH3:14])=[C:6]([CH2:10][CH2:11][CH3:12])[CH:7]=1)(=[O:18])[CH2:16][CH3:17]

Participants

Reactant 2

HCID 62324Propionyl chloride

HCID 14665561HCID 14665561, compound

Product 1

HCID 20185249HCID 20185249, compound

Procedure

2,6-Di-n-propylanisole and propionyl chloride were treated in the same way as in step (a) of Example 30 to give 4-propionyl-2,6-di-n-propylanisole.

Sources & evidence

ORD record: ord-94991bd1446e47529c434117dcb7dd48
Source dataset: uspto-grants-1987_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04695581

Reaction notes

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