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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095518Generated: October 31, 2026

Dimethyl Sulfoxide → 3-[(3-Chloro-4-trifluoromethoxy-phenyl)-(2-oxo-ethyl)-amino]-propionic acid tert-butyl ester

https://huagongshe.com/reaction/2095518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantMonobasic potassium phosphateHCID 516951—
Reactant3-[(3-Chloro-4-trifluoromethoxy-phenyl)-(2-hydroxy-ethyl)-amino]-propionic acid tert-butyl esterHCID 67074007—
SolventDichloromethaneHCID 6344—
Product3-[(3-Chloro-4-trifluoromethoxy-phenyl)-(2-oxo-ethyl)-amino]-propionic acid tert-butyl esterHCID 86652690—

Reaction Conditions

Temperature-5 °C

Reaction Steps

To a solution of 0.55 ml (6.3 mmol) of oxalyl chloride in 21 ml CH2Cl2 at −50 to −60° C. was added a solution of 0.93 ml (13.1 mmol) dimethylsulfoxide in 7 ml of CH2Cl2 within 20 min. The solution was stirred for 5 min, then a solution of 2.10 g (5.5 mmol) of 3-[(3-chloro-4-trifluoromethoxy-phenyl)-(2-hydroxy-ethyl)-amino]-propionic acid tert-butyl ester in 14 ml CH2Cl2 was added within 20 min. The mixture was stirred for 15 min and 3.81 ml (27.4 mmol) of triethylamine were added within 20 min. The suspension was stirred for 3 h and slowly warmed to −5° C. The reaction was neutralized with cold aqueous 10% KH2PO4 (adjusted with solid KH2PO4 to pH 4-5) and extracted with EtOAc (3×). The organic phases were washed with aqueous saturated NaHCO3 (freshly prepared), aqueous 10% NaCl, dried over Na2SO4 evaporated to yield 2.21 g (quantitative) of the title compound as yellow oil. MS: 381 (M+, Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445674B2
Source datasetuspto-grants-2013_05
ORD IDord-9bdc09a5c69d47f0b58fb9d763f4e6df
Source noteuspto-grants-2013_05