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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40838Generated: October 29, 2026

Diethyl Ether → (R)-4-(1-Aminoethyl)cyclohexan-1-ol

https://huagongshe.com/reaction/40838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant(R)-tert-butyl 1-(4-hydroxycyclohexyl)ethylcarbamateHCID 59414492—
SolventDichloromethaneHCID 6344—
Product(R)-4-(1-Aminoethyl)cyclohexan-1-olHCID 55285649—

Reaction Steps

Tert-butyl (R)-1-(4-hydroxycyclohexyl)ethylcarbamate (4.49 g, 18.45 mmol) was dissolved in dichloromethane (25 mL) and cooled to 0° C. under nitrogen. HCl 2M in Ether (27.68 mL of 2 M, 55.35 mmol) was added and the reaction allowed to warm slowly to ambient temperature for 18 hours. The reaction mixture was concentrated in vacuo. The crude mixture was dissolved in MeOH (25 mL). MP-Carbonate was added (11.75 g, 36.90 mmol) and the reaction mixture was stirred for 3 hours. The resin was filtered and the mother liquors were concentrated to dryness to afford the title compound as an off white solid (2.39 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530489B2
Source datasetuspto-grants-2013_09
ORD IDord-bc8d9b1309e74fb5a1f1c765ba87bee4
Source noteuspto-grants-2013_09