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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976946Generated: October 31, 2026

2,6-Dichlorobenzoyl chloride → (S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester

https://huagongshe.com/reaction/1976946

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-N-((1,1-dimethylethoxy)carbonyl)-L-phenylalanine methyl esterHCID 11011855—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl esterHCID 54393861100.3%

Reaction Steps

To a solution of 4-amino-N-[(1,1-dimethylethoxyl)carbonyl]-L-phenylalanine methyl ester 2.6 g, 8.6 mmol) in dichloromethane (20 mL) were added diisopropylethylamine (2.3 mL, 13 mmol) followed by 2,6-dichlorobenzoyl chloride (1.99 g, 9.5 mmol) at room temperature. The mixture was stirred for 15 hr at which time a white precipitate formed. The mixture was diluted with 30 mL of dichloromethane and 50 mL of water. The layers were separated and the aqueous layer was extracted with dichloromethane (2×50 mL). The combined extracts were washed with brine and dried over anhydrous magnesium sulfate. Filtration and concentration of the solvent gave 4.03 g (quant) of 4-[(2,6-dichlorophenylcarbonyl)amino]-N-[(1,1-dimethylethoxyl)carbonyl]-L-phenylalanine methyl ester as a white solid: mp 148-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06229011B1
Source datasetuspto-grants-2001_05
ORD IDord-99ef85d0e1e44c8a8b5d7b071d86be03
Source noteuspto-grants-2001_05