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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45255Generated: October 28, 2026

Water → tert-butyl {(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}carbamate

https://huagongshe.com/reaction/45255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactanttert-butyl N-((1R,3S)-3-(hydroxymethyl)cyclopentyl)carbamateHCID 11962831—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl {(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}carbamateHCID 8665974975%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1.4 g (6.7 mmol) of tert-butyl [(1R,3S)-3-(hydroxymethyl)cyclopentyl]carbamate in 20 mL of anhydrous THF are added portionwise under argon, at room temperature, 0.27 g (6.7 mmol) of sodium hydride at 60% in oil. After stirring for 45 minutes, the medium is cooled to 0° C. and 0.8 mL (6.7 mmol) of benzyl bromide is added. After stirring for 1 hour at room temperature, the medium is hydrolysed with 30 mL of water and extracted with 2×100 mL of EtOAc, dried over Na2SO4, concentrated under reduced pressure and then purified by chromatography on a column of silica gel, eluting with a 99/1 DCM/MeOH mixture. 1.53 g of tert-butyl {(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}carbamate are obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541455B2
Source datasetuspto-grants-2013_09
ORD IDord-da404e7ae40b4427b191215eb8aa30fd
Source noteuspto-grants-2013_09