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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180978Generated: October 27, 2026

Triethylamine → (R)-2-(((Benzyloxy)carbonyl)amino)pentane-1,5-diyl dimethanesulfonate

https://huagongshe.com/reaction/1180978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant(R)-Benzyl (1,5-dihydroxypentan-2-yl)carbamateHCID 2757382—
SolventDichloromethaneHCID 6344—
Product(R)-2-(((Benzyloxy)carbonyl)amino)pentane-1,5-diyl dimethanesulfonateHCID 66524788—

Reaction Steps

A solution of benzyl(1R)-4-hydroxy-1-(hydroxymethyl)butylcarbamate (1.5 g) in DCM (60 ml) was treated with triethylamine (3.3 ml) and stirred at room temperature for 10 min. Methanesulphonyl chloride (1.34 ml) was then added dropwise and the resultant mixture stirred at 0° C. for 75 min. Sodium bicarbonate solution was added and the reaction mixture allowed to reach room temperature over 1 h. The organic layer was separated, washed with brine, dried (over magnesium sulphate) and concentrated under reduced pressure to give a yellow oil. The oil was purified using Biotage™ chromatography (eluting with hexane:ethyl acetate 1:2, 1:3) to give the title compound (1.924 g) as a yellow oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282497B2
Source datasetuspto-grants-2007_10
ORD IDord-a337d4bfb19944f182aeebcb6f98f997
Source noteuspto-grants-2007_10