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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28828Generated: October 28, 2026

Triethylamine → HCID 68852565, compound

https://huagongshe.com/reaction/28828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant(3-Chlorophenyl)(2-hydroxycyclohexyl)acetic acidHCID 68855017—
SolventDichloromethaneHCID 6344—
ProductHCID 68852565HCID 68852565—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (3-chlorophenyl)(2-hydroxycyclohexyl)acetic acid (Reference Example 2-d) (1.25 g, 4.66 mmol), benzotriazol-1-yloxytris(dimethylaminop)phosphonium hexafluorophosphate (3.1 g, 7.0 mmol), and tert-butyl 1-piperazinecarboxylate (0.87 g, 4.66 mmol) in methylene chloride (12 mL) was treated with triethylamine (0.98 mL, 7.0 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 25% EtOAc/hexane) to yield 0.97 g (83%) the lactone, 3-(3-chlorophenyl)hexahydro-1-benzofuran-2(3H)-one as a clear oil. HRMS: calcd for C14H15ClO2+H, 251.0861; found (ESI, [M+H]+), 251.0844.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419980B2
Source datasetuspto-grants-2008_09
ORD IDord-028306892bfc4acf8f5baa7e64649716
Source noteuspto-grants-2008_09