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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7287Generated: October 26, 2026

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

https://huagongshe.com/reaction/7287

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 numberUS07084139B2
Source datasetuspto-grants-2006_08
ORD IDord-f0d992a9a8f14e6b9e4f8b4467f7e8d6
Source noteuspto-grants-2006_08