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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387572Generated: October 31, 2026

Triethylamine → HCID 86609879, compound

https://huagongshe.com/reaction/2387572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
ReactantHCID 57754831HCID 57754831—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 86609879HCID 86609879—

Reaction Steps

A solution of 10 g (5R)-3-(4-benzyloxy-3-fluoro-phenyl)-5-hydroxymethyl-oxazolidin-2-one (MW: 317.32, 31.51 mmol) and 4.78 g triethylamine (MW: 101.19, 47.26 mmol) in 300 ml dichloromethane was treated under stirring at 10° C. with 4.32 g of methane sulfonyl chloride (MW: 114.55, 37.82 mmol). The reaction was stirred at room temperature for one hour and monitored by TLC (ethyl acetate:hexane 1:1). The reaction mixture was quenched with 100 ml water and the organic layer washed with 100 ml brine. The organic layer was dried over magnesium sulfate, filtered and the filtrate evaporated under reduced pressure. The residue was dissolved in 100 ml dimethylformamide, 5.12 g sodium azide (MW: 65.01, 78.7 mmol) and a catalytic amount of tetrabutyl ammonium iodide were added. The suspension was stirred at 90° C. over night. The reaction was monitored by HPLC. The dimethylformamide was evaporated under reduced pressure, the residue dissolved in 200 ml dichloromethane and the organic layer washed successively with 100 ml water and 100 ml brine. The dichloromethane solution was dried over magnesium sulfate, filtered, and the filtrate evaporated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268812B2
Source datasetuspto-grants-2012_09
ORD IDord-7ead71f2ad9a451e95b3636ac8910b25
Source noteuspto-grants-2012_09