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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556879Generated: October 30, 2026

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

https://huagongshe.com/reaction/556879

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 numberUS08058045B2
Source datasetuspto-grants-2011_11
ORD IDord-483ba880640e45009ead47f8d4e49d4c
Source noteuspto-grants-2011_11