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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366989Generated: November 1, 2026

Triethylamine → HCID 11237168, compound

https://huagongshe.com/reaction/2366989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Hydroxy-4-phenylcyclohexan-1-oneHCID 583741—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 57803383HCID 57803383—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11237168HCID 11237168—

Reaction Steps

To a solution of the pyrrolidine intermediate from step C (0.3 g, 0.85 mmol) and the ketone from step E (0.16 g, 0.85 mmol) in THF (5 mL) was added Na(OAc)3BH (0.35 g, 2.5 mmol) followed by triethylamine (0.2 mL, 1.5 mmol). The reaction was continued at room temperature overnight and quenched by addition of a saturated NaHCO3 solution. The resulting solution was extracted with EtOAc and the EtOAc layer was dried over MgSO4 and concentrated. Separation on silica gel eluting with 10% to 30% MeOH/EtOAc provided the cis (fast moving spot) and trans (slow moving spot) isomers of the title compound. MS (M+H)+ 490.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697870B2
Source datasetuspto-grants-2014_04
ORD IDord-e60a3c365a4444af83c56266f23f06e4
Source noteuspto-grants-2014_04