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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233259Generated: October 30, 2026

Triethylamine → HCID 86761097, compound

https://huagongshe.com/reaction/2233259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Boc-3-pyrrolidinolHCID 4416939—
SolventDiethyl EtherHCID 3283—
ProductHCID 86761097HCID 86761097191.3%

Reaction Steps

Triethylamine (4.5 ml, 32.0 mmol) was added to a stirred solution of, N-(tert-butoxy-carbonyl)-3-hydroxypyrrolidine (2.00 g, 10.7 mmol) in diethyl ether (100 ml) and the reaction was cooled to 0° C. before addition of methanesulphonyl chloride (1.65 ml, 21.4 mmol) and stirring for 2 hours, warming from 0° C. to ambient temperature. The reaction was filtered, the filtrate was washed with 1.0 N hydrochloric acid (100 ml) and with brine (100 ml) before being dried over magnesium sulphate. Solvent evaporation in vacuo yielded N-(tert-butoxycarbonyl)-3-hydroxypyrrolidine methanesulphonate (2.9 g, 100% yield) as a colourless oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709479B1
Source datasetuspto-grants-2010_05
ORD IDord-d6384683522e401cadb1a8953d93b1d3
Source noteuspto-grants-2010_05