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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733272Generated: October 25, 2026

Butylamine → Ethyl 3-(2-butyl-carbamoylphenyl)-2-methylacrylate

https://huagongshe.com/reaction/733272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylamineHCID 8007—
ReactantTriethylamineHCID 8471—
ReactantO-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733286—
Reactant2-(2-Ethoxycarbonylpropen-1-yl)benzoic acidHCID 69054538—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-(2-butylcarbamoylphenyl)-2-methylacrylateHCID 69055256—
ProductEthyl 3-(2-butyl-carbamoylphenyl)-2-methylacrylateHCID 69055262156.2%

Reaction Steps

Ethyl 3-(2-butylcarbamoylphenyl)-2-methylacrylate is prepared as described in Example 30, starting with 1.17 g (5.0 mmol) of 2-(2-ethoxycarbonylpropen-1-yl)benzoic acid in 10 cm3 of dimethylformamide, a solution of 0.69 cm3 (5.0 mmol) of triethylamine, 1.64 g (5.0 mmol) of O-[(cyano(ethoxycarbonyl)methylene)amino]-1,1,3,3-tetramethyluronium tetrafluoroborate (“TOTU”) in 6 cm3 of dimethylformamide and a second solution consisting of 366 mg (5.0 mmol) of n-butylamine and 0.69 cm3 (5.0 mmol) of triethylamine in 10 cm3 of dimethylformamide. 1.13 g of ethyl 3-(2-butyl-carbamoylphenyl)-2-methylacrylate are thus obtained in the form of a yellowish oil, which can be reacted in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589117B2
Source datasetuspto-grants-2009_09
ORD IDord-0205f39e4f1547bc8bcf8a6663c981a8
Source noteuspto-grants-2009_09