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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168115Generated: November 1, 2026

Triethylamine → HCID 22991103, compound

https://huagongshe.com/reaction/1168115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactanttert-Butyl (((1,1-dimethylethoxy)carbonyl)oxy)carbamateHCID 2728863—
SolventDichloromethaneHCID 6344—
ProductHCID 22991103HCID 2299110328%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of acryloyl chloride (700 μL; 779.8 mg; 8.6 mmole) dissolved in dry dichloromethane (20 mL) was cooled at 0° C. with an ice bath. A mixture of tert-butyl N-(tert-butoxycarbonyloxy)carbamate (31) (2.0038 g; 8.6 mmole) and triethylamine (1.32 mL; 958.3 mg; 9.5 mmole) in dry dichloromethane (20 mL) was slowly added over a period of 1 hour to the cooled solution. The ice bath was removed after 4 hours and the reaction mixture was left stirring overnight while its temperature warmed up gradually to room temperature. Water (100 mL) was added to the reaction and the layers were separated. The organic solution was washed with a 10% ammonium chloride solution (3×80 mL), water (2×100 mL), and finally brine (1×100 mL). The organic layer was then dried over magnesium sulfate, filtered, and the solvent removed under reduced pressure. The residue was purified by flash chromatography using a mixture of hexane and ethyl acetate (90:10) to elute the product. The purification gave 690 mg (28%) of N-(tert-butoxycarbonyl),N-(tert-butoxycarbonyloxy)acrylamide (32) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06623721B2
Source datasetuspto-grants-2003_09
ORD IDord-5f6f6d2be631449dae8d40a48041711c
Source noteuspto-grants-2003_09