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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174376Generated: November 1, 2026

Triethylamine → tert-butyl 3-methyl-N-(methylsulfonyl)-L-valinate

https://huagongshe.com/reaction/1174376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantL-(+)-Ttert-butyl tert-leuc-inateHCID 11252445—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Producttert-butyl 3-methyl-N-(methylsulfonyl)-L-valinateHCID 86599586100%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of tert-butyl 3-methyl-L-valinate (50 mg, 0.223 mmol) in dichloromethane (1 mL) at 0° C. was treated with 4-(dimethylamino)pyridine (5.4 mg, 0.045 mmol), triethylamine (93.4 μL, 0.67 mmol), and methanesulfonyl chloride (34.5 L, 0.45 mmol), and the mixture was warmed to 25° C. for 1 h. The mixture was washed with 5% potassium bisulfate, saturated sodium bicarbonate, brine, and dried over MgSO4, filtered, and the solvents were evaporated to give the crude title compound (59 mg, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834043B2
Source datasetuspto-grants-2010_11
ORD IDord-36a2dcb7615d4057b1f4c40e17389e13
Source noteuspto-grants-2010_11