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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20370Generated: October 25, 2026

1-Nitro-2-phenylethane → 2(S)-(2-Cyclohexylethyl)-5-(R)-(1-(R)-hydroxy-2-(S)-nitro-3-phenylpropyl)-morpholine-4-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/20370

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Nitro-2-phenylethaneHCID 80208—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-(S)-(2-Cyclohexylethyl)-5-(R)-formylmorpholine-4-carboxylic acid tert-butyl esterHCID 86615361—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2(S)-(2-Cyclohexylethyl)-5-(R)-(1-(R)-hydroxy-2-(S)-nitro-3-phenylpropyl)-morpholine-4-carboxylic acid tert-butyl esterHCID 6855820463.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Add 1-phenyl-2-nitroethane (91 mg, 0.61 mmol) to a solution of 2-(S)-(2-cyclohexylethyl)-5-(R)-formylmorpholine-4-carboxylic acid tert-butyl ester (164 mg, 0.50 mmol) in dry tetrahydrofuran (6 mL). Cool to 0° C. and add tetrabutylammonium fluoride (0.25 mL of a 1 M solution in tetrahydrofuran, 0.25 mmol) and refrigerate the solution overnight. Dilute with ethyl acetate, wash with cold saturated aqueous sodium chloride (50 mL), dry (sodium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 2.5:97.5 ethyl acetate:dichloromethane) to give the desired compound as a white foam (152 mg, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745438B2
Source datasetuspto-grants-2010_06
ORD IDord-d78273dba6dc49e19ac8e515be59185f
Source noteuspto-grants-2010_06