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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383772Generated: October 31, 2026

Acetic Acid → HCID 54188068, compound

https://huagongshe.com/reaction/1383772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514397—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-(4-Fluorophenyl)-4-hydroxycyclohexan-1-oneHCID 22395364—
SolventMethanolHCID 887—
SolventIsopropanol ethyl acetateHCID 22055037—
ProductHCID 54188068HCID 5418806856%

Reaction Steps

To a solution of 4-(4-Fluorophenyl)-4-hydroxy-cyclohexanone (2.0 g, 9.6 mmol) and acetic acid (2.6 ml, 48 mmol) in methanol (60 Ml) was added (3R)-(+)-3-(tert-butoxycarbonyl amino) pyrrolidine (2.6 g, 14.4 mmol). After stirring for 2 hours at room temperature, sodium cyanoborohydride (1M in tetrahydrofuran, 14.4 ml, 14.4 mmol) was added dropwise. The reaction mixture was stirred for 45 minutes, concentrated, diluted with 10% potassium hydrogen sulfate and extracted twice with ether. The aqueous solution was sasified with 1N sodium hydroxide and extracted with ethyl acetate three times. Washing with brine, drying and solvent evaporation gave an oil. Flash chromatography (silica gel, 2-propanol-ethyl acetate, 4:96 increasing to 8:92) gave 4-(3-(3R)-tert-Butoxycarbonylamino-pyrrolidin-1-yl)-1-(4-fluorophenyl)-cyclohexanol (2.0 g, 56%); 1H NMR (CDCl13) δ 7.46(m, 2H), 7.02 (m, 2H), 4.89 (m, 1H), 4.18 (m, 1H), 2.94 (m, 1H), 2.71 (m, 2H), 2.42 (m, 1H), 2.26 (m, 1H), 2.13 (m, 1H), 1.83 (m, 9H), 1.63 (m, 1H), 1.44 (s, 9H),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255315B1
Source datasetuspto-grants-2001_07
ORD IDord-33f3c36e55e64ed28ae907217392f475
Source noteuspto-grants-2001_07