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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384714Generated: October 31, 2026

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

https://huagongshe.com/reaction/384714

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 sulphonyl 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 numberUS08367658B2
Source datasetuspto-grants-2013_02
ORD IDord-e2344e7844c04e1a91c8972ef82fb80f
Source noteuspto-grants-2013_02