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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853463Generated: October 31, 2026

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

https://huagongshe.com/reaction/1853463

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 numberUS08962642B2
Source datasetuspto-grants-2015_02
ORD IDord-dae4c4d4145c4bf890463e7421570468
Source noteuspto-grants-2015_02