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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706967Generated: October 30, 2026

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

https://huagongshe.com/reaction/706967

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 numberUS09174982B2
Source datasetuspto-grants-2015_11
ORD IDord-435583a5ceb14ddb9c313e5166b076e0
Source noteuspto-grants-2015_11