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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710766Generated: November 3, 2026

Triethylamine → HCID 59457456, compound

https://huagongshe.com/reaction/1710766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(2-CHLOROOXAZOL-4-YL)METHANOLHCID 11378512—
SolventDichloromethaneHCID 6344—
ProductHCID 59457456HCID 59457456—

Reaction Steps

A solution of (2-chloro-1,3-oxazol-4-yl)methanol (5 g, 37.44 mmol, 1 eq, prepared according to the method described in Tetrahedron Lett. (2004), 45, 3797-3802) in dichloromethane (250 ml) is reacted with methanesulfonyl chloride (3.19 ml, 41.19 mmol, 1.1 eq) in the presence of triethylamine (5.79 ml, 41.19 mmol, 1.1 eq) at 0° C. After 1 h 30, the mixture is poured into a saturated solution of ammonium chloride and extracted twice with dichloromethane. The organic layer is dried over magnesium sulfate, filtered and concentrated under vacuum to afford 7.9 g of (2-chloro-1,3-oxazol-4-yl)methyl methanesulfonate i59. This product is used in the next step without further purification or analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790720B2
Source datasetuspto-grants-2010_09
ORD IDord-65ec77fffeb0425fbc48b518f79e7c44
Source noteuspto-grants-2010_09