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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28802Generated: October 26, 2026

Triethylamine → Tert-butyl 4-[(3-chlorophenyl)(1-hydroxycyclohexyl)acetyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/28802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant(3-Chlorophenyl)(1-hydroxycyclohexyl)acetic acidHCID 68853928—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-[(3-chlorophenyl)(1-hydroxycyclohexyl)acetyl]piperazine-1-carboxylateHCID 6885600381%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (3-chlorophenyl)(1-hydroxycyclohexyl)acetic acid (Reference Example 1-a) (5.4 g, 20.1 mmol), benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (14.22 g, 32.15 mmol), and tert-butyl 1-piperazinecarboxylate (5.99 g, 32.15 mmol) in methylene chloride (20 mL) was treated with triethylamine (8.4 mL, 60.3 mmol). The reaction was stirred at 25° C. for 16 h, after which time the solvent was removed in vacuo and the product was purified via Biotage Horizon (FLASH 40 M, silica, gradient from 0% EtOAc/hexane to 30% EtOAc/hexane) to yield 7.10 g (81%) tert-butyl 4-[(3-chlorophenyl)(1-hydroxycyclohexyl)acetyl]piperazine-1-carboxylate as a white foam. HRMS: calcd for C23H33ClN2O4, 436.2129; found (ESI_FT), 437.21996.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419980B2
Source datasetuspto-grants-2008_09
ORD IDord-06374a6a707b482680fd93a0cfde0229
Source noteuspto-grants-2008_09