Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41013Generated: October 29, 2026

Diethyl Ether → tert-butyl N-{[1-(hydroxymethyl)cyclopentyl]methyl}carbamate

https://huagongshe.com/reaction/41013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantMethyl 1-[(tert-butoxycarbonyl)amino]methylcyclopentanecarboxylateHCID 57478043—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-{[1-(hydroxymethyl)cyclopentyl]methyl}carbamateHCID 5747804477%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of methyl 1-[(tert-butoxycarbonyl)amino]methylcyclopentanecarboxylate (1.50 g, 5.83 mmol) in THF (25.0 mL) at −78° C. was added dropwise 1.0 M diisobutylaluminum hydride in DCM (17.5 mL). The reaction was stirred for 2 hours with slow warming to −10° C. A saturated solution of K/Na tartrate was added, followed by ether. This mixture was stirred for 30 minutes at ambient temperature and the organic layer was separated and washed with water, and brine. The organic layer was then dried over sodium sulfate, and the solvent was removed in vacuo to afford the product (1.03 g, 77%). 1H NMR (300 MHz, CDCl3): δ □4.90 (br s, 1H), 3.27 (s, 2H), 3.06 (d, 2H), 1.5-1.17 (m, 8H), 1.44 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530485B2
Source datasetuspto-grants-2013_09
ORD IDord-4d12306b14624c5e8cb9c2f0950e1b66
Source noteuspto-grants-2013_09