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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417977Generated: November 2, 2026

Triethylamine → HCID 178505302, compound

https://huagongshe.com/reaction/2417977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 178521098HCID 178521098—
SolventDichloromethaneHCID 6344—
ProductHCID 178505302HCID 178505302—

Reaction Steps

A solution of 2(S)-glycerol-2,3-acetonide (109 g), obtained from mannitol-1,2:5,6-diacetonide via D-glyceraldehyde acetonide using the method described by LeCocq et al., Biochem., 3, 976 (1964), in 1 L dry dichloromethane was cooled to -35° with stirring. Triethylamine (140 ml) was added followed by the dropwise addition of mesyl chloride (71 ml) over 10 minutes while maintaining the reaction between -35° and -25°. The cooling bath was removed and after 45 minutes, 250 ml 1N hydrochloric acid was added. The layers were separated and the dichloromethane solution was washed in turn with 250 ml portions of water (1×), 1N sodium hydroxide (1×) and water (1×). The aqueous layers were dried over sodium sulfate and evaporated to give 172.1 g of (2R)-3-mesyloxy-1,2-propanediol acetonide as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04471116
Source datasetuspto-grants-1984_09
ORD IDord-17496b13ed4646cf8d299d6ea26c4c4f
Source noteuspto-grants-1984_09