Benzoyl chloride → HCID 22768162, compound

HRID 1763201Notes

Reaction equation

HRID 1763201 reaction equation
[NH2:1][C:2]1[CH:6]=[C:5]([C:7]([CH3:10])([CH3:9])[CH3:8])[O:4][N:3]=1.[C:11](Cl)(=[O:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C1C=CC=CC=1.N1C=CC=CC=1>[C:11]([NH:1][C:2]1[CH:6]=[C:5]([C:7]([CH3:10])([CH3:9])[CH3:8])[O:4][N:3]=1)(=[O:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

Participants

5

Reactant 2

HCID 7412Benzoyl chlorideHCID 1714733-Isoxazolamine, 5-(1,1-dimethylethyl)-

Product 1

HCID 22768162HCID 22768162, compound

Reagents, catalysts & solvents 2

HCID 241BenzeneSolventHCID 1049PyridineSolvent

Procedure

To a solution of 3-amino-5-t-butylisoxazole in benzene, benzoyl chloride and pyridine are added, whereby the reaction is carried out. Thus 3-benzoylamino-5-t-butylisoxazole is obtained as crystals melting at 192° to 193° C.

Sources & evidence

ORD record
ord-63a53d5df2244b5e9653594136d2309d
Source dataset
uspto-grants-1978_09
Patent number
US04111680

Reaction notes

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