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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682928Generated: November 2, 2026

Benzhydrylamine → HCID 54108237, compound

https://huagongshe.com/reaction/1682928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrylamineHCID 7036—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 54402920HCID 54402920—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 54108237HCID 5410823780%

Reaction Steps

To a suspension of (+)-(4aR)-(10bR)-4-methyl-8-(3-formylphenyl)-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one (30 mg, 0.09 mmol), in 0.75 mL of methanol was added benzhydrylamine (0.09 mmol), sodium cyanoborohydride (0.09 mmol) and 2 drops of glacial acetic acid (mixture became homogeneous; pH=4). The reaction was stirred at room temperature for 60 h. The mixture was diluted with ethyl acetate, saturated aqueous sodium bicarbonate solution was added, and the resulting mixture was extracted repeatedly with ethyl acetate. The combined organic extracts were dried over sodium sulfate, concentrated, and purified by silica gel chromatography (ethyl acetate eluent), followed by trituration of the resulting oil with ether/hexanes, to give 36 mg (80%) of the title compound as a white solid. mp 55°-57° FDMS: m/e =500. α[D]589 =+48.40 (c=0.64, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05635197
Source datasetuspto-grants-1997_06
ORD IDord-4a64b588267043098a766a38585db7f6
Source noteuspto-grants-1997_06