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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045903Generated: October 31, 2026

Dimethylformamide → 4-[(2S)-4-[(1R)-1-phenylethyl]morpholin-2-yl]benzaldehyde

https://huagongshe.com/reaction/2045903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant(2S)-2-(4-bromophenyl)-4-[(1R)-1-phenylethyl]morpholineHCID 50992522—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-[(2S)-4-[(1R)-1-phenylethyl]morpholin-2-yl]benzaldehydeHCID 59317736101.9%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of (2S)-2-(4-bromophenyl)-4-((1R)-1-phenylethyl)morpholine (intermediate 7, 63.3 g, 183 mmol) in tetrahydrofuran (450 ml) was added n-butyllithium (1.57 M in hexane solution, 175 ml, 275 mmol) at −78° C. and the mixture was stirred for 20 minutes. N,N-dimethylformamide (28.3 ml 365 mmol) was added and the mixture was stirred for 2 hours at −78° C. and then allowed to be warmed to −10° C. The reaction was quenched with aqueous ammonium chloride, and the resulting solution was partitioned between water and ethyl acetate. The organic layer was washed with water and brine and dried over sodium sulfate. The solvent was evaporated under reduced pressure to afford crude 4-((2S)-4-((1R)-1-phenylethyl) morpholin-2-yl)benzaldehyde (intermediate 8, 55.1 g). This compound was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592417B2
Source datasetuspto-grants-2013_11
ORD IDord-06bb460f06ba4df7a68fb6f5a077a337
Source noteuspto-grants-2013_11