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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556874Generated: October 30, 2026

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

https://huagongshe.com/reaction/556874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
Reactanttert-Butyl (2S)-2-(hydroxymethyl)morpholine-4-carboxylateHCID 1512577—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(S)-tert-Butyl 2-((tosyloxy)methyl)morpholine-4-carboxylateHCID 5404363897.8%

Reaction Steps

Toluene suiphonyl chloride (0.513 g, 2.69 mmol) was added to a solution of (S)-tert-butyl 2-(hydroxymethyl)morpholine-4-carboxylate (0.390 g, 1.79 mmol), triethylamine (0.50 mL, 3.59 mmol) and DMAP (cat.) in dichloromethane (11 mL). The reaction mixture was stirred for 24 h then diluted with dichloromethane (25 ml) and washed sequentially with water (25 mL) and 0.2M HCl (25 mL). The organic phase was dried (Na2SO4) and the solvent was removed in vacuo. The crude product was purified by flash column chromatography on silica gel, eluting with ethyl acetate/hexane (1/5), to give the title compound as a colourless solid (0.650 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058045B2
Source datasetuspto-grants-2011_11
ORD IDord-ca75f430e0e647dcaceb6cf6356b981a
Source noteuspto-grants-2011_11