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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096197Generated: October 25, 2026

Dimethyl Sulfoxide → 3-[(3,4-Dichloro-phenyl)-(2-oxo-ethyl)-amino]-propionic Acid tert-butyl ester

https://huagongshe.com/reaction/1096197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantMonobasic potassium phosphateHCID 516951—
Reactant3-[(3,4-Dichloro-phenyl)-(2-hydroxy-ethyl)-amino]-propionic Acid tert-butyl esterHCID 66783234—
SolventDichloromethaneHCID 6344—
Product3-[(3,4-Dichloro-phenyl)-(2-oxo-ethyl)-amino]-propionic Acid tert-butyl esterHCID 8663837899.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1.91 ml (21.77 mmol) of oxalyl chloride in 64 ml CH2Cl2 at −50 to −60° C. was added a solution of 3.22 ml (45.42 mmol) dimethylsulfoxide in 12 ml of CH2Cl2 within 20 min. The solution was stirred for 5 min, then a solution of 6.33 g (18.93 mmol) of 3-[(3,4-dichloro-phenyl)-(2-hydroxy-ethyl)-amino]-propionic acid tert-butyl ester in 43 ml CH2Cl2 was added within 20 min. The mixture was stirred for 15 min and 13.17 ml (94.63 mmol) of triethylamine were added within 20 min. The suspension was stirred for 3 h and slowly warmed to 0° C. The reaction was neutralized with cold aq. 10% KH2PO4 solution (adjusted with solid KH2PO4 to pH 4-5) and extracted with EtOAc (3×). The organic phases were washed with aq. 10% KH2PO4, solution sat. aq. NaHCO3 solution, aq. 10% NaCl solution, dried over Na2SO4 evaporated to yield 6.26 g (99.6%) of the title compound as orange oil. MS: 332.0 (MH+, 2Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138175B2
Source datasetuspto-grants-2012_03
ORD IDord-b889ae4f276446dea2c68f79a0ede20a
Source noteuspto-grants-2012_03