Isobutyryl chloride → HCID 21323681, compound

HRID 1112389Notes

Reaction equation

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

Participants

Reactant 2

HCID 62325Isobutyryl chloride

HCID 12295237HCID 12295237, compound

Product 1

HCID 21323681HCID 21323681, compound

Procedure

2-(N-Butylamino)-4-isopropyloxazole was acylated with isobutyryl chloride as described in Example 9.

Sources & evidence

ORD record: ord-e34e8667ac064dd0a687c662733eb3a3
Source dataset: uspto-grants-1978_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04122183

Reaction notes

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