Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574875Generated: October 28, 2026

4-Toluenesulfonyl chloride → (S)-tert-Butyl 2-((tosyloxy)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/574875

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl (2S)-2-(hydroxymethyl)morpholine-4-carboxylateHCID 1512577—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product(S)-tert-Butyl 2-((tosyloxy)methyl)morpholine-4-carboxylateHCID 54043638—

Reaction Steps

To a solution of (S)-tert-butyl 2-(hydroxymethyl)morpholine-4-carboxylate (1 g) in dichloromethane (50 mL) was added triethylamine (1.604 mL) and 4-methylbenzene-1-sulfonyl chloride (1.097 g). The mixture was stirred at ambient temperature under nitrogen for 72 hours. The reaction was diluted with methylene chloride (50 mL) and brine (100 mL). The brine layer was extracted with methylene chloride (75 mL). The combined organics were dried over sodium sulfate, filtered and concentrated. The crude material was purified on a silica gel column eluting with a 15-65% ethyl acetate in hexane gradient to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034875B2
Source datasetuspto-grants-2015_05
ORD IDord-77865ddb09ff4d03907b26bfc54477de
Source noteuspto-grants-2015_05