Hydrochloric Acid → HCID 20213849, compound

HRID 1906062Notes

Reaction equation

HRID 1906062 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][C:12]=2[Cl:21])=[CH:6][C:5]=1[NH:22][CH2:23][CH2:24][CH2:25][C:26]([O:28][CH3:29])=[O:27])([O-:3])=[O:2].Cl.[C:31](Cl)(=[O:33])[CH3:32]>>[C:31]([N:22]([C:5]1[CH:6]=[C:7]([O:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:18])([F:19])[F:20])=[CH:13][C:12]=2[Cl:21])[CH:8]=[CH:9][C:4]=1[N+:1]([O-:3])=[O:2])[CH2:23][CH2:24][CH2:25][C:26]([O:28][CH3:29])=[O:27])(=[O:33])[CH3:32]

Participants

4

Procedure

10 g of methyl N-[2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenyl]-4-amino-n-butyrate (compound 2) are refluxed in 30 ml of acetyl chloride until the evolution of hydrogen chloride is complete. Excess acetyl chloride is removed in vacuo, affording the title compound in quantitative yield. nD21 =1.5437.

Workup

  1. customExcess acetyl chloride is removed in vacuo

Sources & evidence

ORD record
ord-94ae5161d1bf4c19a222b377c8fb7699
Source dataset
uspto-grants-1987_03
Patent number
US04649212

Reaction notes

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