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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28830Generated: October 29, 2026

tert-Butyl piperazine-1-carboxylate → HCID 68855483, compound

https://huagongshe.com/reaction/28830

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68855467HCID 68855467—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 68855483HCID 68855483274.6%

Reaction Steps

A solution of 3-(3-chlorophenyl)octahydro-1-benzofuran-2-ol (175 mg, 0.69 mmol) and tert-butyl 1-piperazinecarboxylate (128 mg, 0.69 mmol) in dichloroethane (3 mL) was treated with sodium trisacetoxyborohydride (220 mg, 1.04 mmol). The reaction was allowed to stir at room temperature for 16 h. The reaction was then diluted with methylene chloride and washed with a saturated aqueious solution of ammonium chloride (3 times). The organic layer was dried over magnesium sulfate and concentrated in vacuo and the product was purified via Biotage Horizon (FLASH 25 M, silica, gradient from 0% EtOAc/hexane to 30% EtOAc/hexane). This material was dissolved in methanol (0.5 mL) and treated with a saturated methanolic solution of hydrochloric acid (0.5 mL) followed by diethyl ether. After crystallizing in the refrigerator for 16 h, the resulting solid was collected, washed with diethyl ether and dried in vacuo to yield 250 mg (83%) 2-[1-(3-chlorophenyl)-2-piperazin-1-ylethyl]cyclohexanol dihydrochloride as a white solid. HRMS: calcd for C18H27ClN2O+H, 323.18901; found (ESI, [M+H]+), 323.1891.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419980B2
Source datasetuspto-grants-2008_09
ORD IDord-555bac77fe6a4f47b5460df267739f15
Source noteuspto-grants-2008_09