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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401372Generated: October 29, 2026

Aniline → 3-Methyl-N-phenylbut-2-enamide

https://huagongshe.com/reaction/401372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTriethylamineHCID 8471—
Reactant3-Methyl-2-butenoic acidHCID 10931—
ReactantThionyl ChlorideHCID 24386—
Product3-Methyl-N-phenylbut-2-enamideHCID 1238702280%

Reaction Steps

A mixture of 3-methyl-but-2-enoic acid (100 g, 1 mol) and SOCl2 (119 g, 1 mol) was heated at reflux for 3 h. The excess SOCl2 was removed under reduced pressure. CH2Cl2 (200 mL) was added followed by the addition of aniline (93 g, 1.0 mol) in Et3N (101 g, 1 mol) at 0° C. The mixture was stirred at room temperature for 1 h and quenched with HCl (5%, 150 mL). The aqueous layer was separated and extracted with CH2Cl2. The combined organic layers were washed with water (2×100 mL) and brine (100 mL), dried over Na2S O4 and concentrated to give 3-methyl-but-2-enoic acid phenylamide (120 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741925B2
Source datasetuspto-grants-2014_06
ORD IDord-cfeef744ba0d4344aefce71ce10933c2
Source noteuspto-grants-2014_06