4-Chlorobenzoyl chloride → 4-Chloro-N-[2-(furan-3-yl)-2-oxoethyl]benzamide

HRID 235890Notes

Reaction equation

HRID 235890 reaction equation
Cl.[O:2]1[CH:6]=[CH:5][C:4]([C:7]([CH2:9][NH2:10])=[O:8])=[CH:3]1.C(=O)(O)[O-].[Na+].[Cl:16][C:17]1[CH:25]=[CH:24][C:20]([C:21](Cl)=[O:22])=[CH:19][CH:18]=1>>[Cl:16][C:17]1[CH:25]=[CH:24][C:20]([C:21]([NH:10][CH2:9][C:7]([C:4]2[CH:5]=[CH:6][O:2][CH:3]=2)=[O:8])=[O:22])=[CH:19][CH:18]=1

Participants

4

Reactant 3

HCID 85014-Chlorobenzoyl chlorideHCID 516892Sodium BicarbonateHCID 137731212-Amino-1-(furan-3-yl)ethan-1-one--hydrogen chloride (1/1)

Product 1

HCID 137731224-Chloro-N-[2-(furan-3-yl)-2-oxoethyl]benzamideYield 100.5%

Procedure

5 g of (3-furylcarbonyl)methylamine hydrochloride, 6.0 g of sodium bicarbonate and 6.0 g of 4-chlorobenzoyl chloride are treated in the same manner as described in Preparation 1-(1). 8.2 g of N-(4-chlorobenzoyl)-(3-furylcarbonyl)methylamine are thereby obtained. Yield: 100%

Workup

  1. customas described in Preparation 1-(1)

Sources & evidence

ORD record
ord-5844296efd8e4889a254e1556a350f76
Source dataset
uspto-grants-1987_02
Patent number
US04642313

Reaction notes

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