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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747652Generated: October 30, 2026

Acetic Acid → HCID 66797682, compound

https://huagongshe.com/reaction/1747652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 825700HCID 825700—
Reactant(R)-beta-aminophenethyl alcoholHCID 2724025—
ReactantSodium borohydrideHCID 4311764—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
ProductHCID 66797682HCID 6679768290%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a mixture of 5-chloro-3,3-dimethylindan-1-one (4.33 g, 0.0222 mol) and (R)-(−)-2-phenylglycinol (3.2 g, 0.0234 mol) in toluene (200 mL) was added p-toluenesulfonic acid monohydrate (241 mg, 0.00127 mol). The reaction was stirred at reflux (140° C.) under an atmosphere of nitrogen overnight, cooled and diluted with toluene. The mixture was washed with saturated aqueous NaHCO3 and water and the organic phase was concentrated. The residue was dissolved in THF (200 mL) under an atmosphere of nitrogen and cooled at 0° C. To this was added acetic acid (3.79 mL, 0.0667 mol) and sodium borohydride (1.26 g, 0.0334 mol). The reaction was stirred under at atmosphere of nitrogen overnight. The reaction was partitioned between CH2Cl2 and saturated aqueous NaHCO3 solution, separated, and the organic phase was evaporated. The residue was purified by flash chromatography (20 to 100% EtOAc/hexanes) to afford the title compound (6.25 g, 90%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150525B2
Source datasetuspto-grants-2015_10
ORD IDord-a76820da855f4680960fc335c4ca808c
Source noteuspto-grants-2015_10