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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963425Generated: October 31, 2026

Triethylamine → HCID 178472005, compound

https://huagongshe.com/reaction/963425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-2-methyl-1-propanolHCID 11807—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 54513699HCID 54513699—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178472005HCID 17847200592%

Reaction Steps

3.6 g of ethyl 2-(4-bromo-2-chloro-benzoyl)-3-dimethylaminoacrylate (Example 13bk)) and 2-amino-2-methyl-1-propanol in 40 ml of 1,2-dichloroethane were stirred at room temperature for 1 hr. with the direct introduction of argon. Then, 0.74 ml of triethylamine, 1.66 g of tert.-butyldimethylchlorosilane and 1.22 mg of 4-dimethylaminopyridine were added and the mixture was stirred at room temperature for 24 hrs. The reaction mixture was chromatographed directly on silica gel in dichloromethane. 4.64 g (92%) of ethyl 2-(4-bromo-2-chloro-benzoyl)-3-[2-(tert.-butyl-dimethyl-silanyloxy)-1,1-dimethyl-ethylamino]-acrylate were obtained as a colourless oil. Mass spectrum (ISP): peaks inter alia at 520 (M+H, 100%), 518 (75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763450
Source datasetuspto-grants-1998_06
ORD IDord-dc5756ae98c0425bbbc21bf2305d9a1f
Source noteuspto-grants-1998_06