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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384719Generated: October 27, 2026

Triethylamine → (R)-tert-butyl 2-(tosyloxymethyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/384719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
Reactant(R)-N-Boc-2-hydroxymethylmorpholineHCID 1512576—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(R)-tert-butyl 2-(tosyloxymethyl)morpholine-4-carboxylateHCID 5404363988.4%

Reaction Steps

Toluene sulphonyl chloride (0.473, 2.48 mmol) was added to a solution of (R)-tert-butyl 2-(hydroxymethyl)morpholine-4-carboxylate (0.360, 1.65 mmol), triethylamine (0.45 mL, 3.30 mmol) and DMAP (cat.) in dichloromethane (10 mL). The reaction mixture was stirred for 24 h then diluted with dichloromethane (20 mL) and washed sequentially with water (20 mL) and 0.2M HCl (20 mL). The organic phase was dried (Na2SO4) and 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 (0.542 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367658B2
Source datasetuspto-grants-2013_02
ORD IDord-81b42a7935e0419aa9f05f24d1356684
Source noteuspto-grants-2013_02