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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772763Generated: November 2, 2026

Dimethyl Sulfoxide → tert-Butyl 4-(2-oxoethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1772763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantTert-butyl 4-(2-hydroxyethyl)piperazine-1-carboxylateHCID 735736—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(2-oxoethyl)piperazine-1-carboxylateHCID 16737781—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Oxalyl chloride (3.6 mL, 0.0425 mol) was dissolved in DCM (87 mL) at −78° C. Dimethyl sulfoxide (6.58 mL, 0.0927 mol) was added and the solution was held at −78° C. for 10 min. To the resultant mixture was added a solution of tert-butyl 4-(2-hydroxyethyl)piperazine-1-carboxylate (from Oakwood, 8.90 g, 0.0386 mol) in DCM (44 mL) over 15 min. The reaction was stirred at −78° C. for 1 h, then triethylamine (26.9 mL, 0.193 mol) was added. The mixture was warmed to RT over 30 minutes and then stirred at RT for another 30 min. The mixture was diluted with DCM, washed with water (2×), brine (1×), dried over sodium sulfate, and concentrated. The crude product (8.10 g, 91.8%) was used directly in next step without further purification. 1H NMR (400 MHz, CDCl3): δ 9.70 (1H, s), 3.48 (4H, m), 3.19 (2H, s), 2.47 (4H, m), 1.45 (9H, s) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249145B2
Source datasetuspto-grants-2016_02
ORD IDord-7320ccdd35ed4939a854787b55a09ea6
Source noteuspto-grants-2016_02