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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710247Generated: October 29, 2026

Dimethylformamide → tert-butyl (2S)-2-(4-cyanophenyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/710247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactanttert-butyl (2S)-2-(4-bromophenyl)morpholine-4-carboxylateHCID 58097875—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
Producttert-butyl (2S)-2-(4-cyanophenyl)morpholine-4-carboxylateHCID 6686140969%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of (S)-tert-butyl 2-(4-bromophenyl)morpholine-4-carboxylate (400 mg, 1.17 mmol), tetrakis(triphenylphosphine)palladium(0) (405 mg, 0.35 mmol) and zinc cyanide (206 mg, 1.75 mmol) in dimethylformamide (6 ml) was degassed with argon and heated in a closed tube at 85° C. on a Büchi shaker overnight. After cooling water (30 ml) was added, and the reaction mixture was extracted with ethyl acetate (50 ml). The aqueous phase was re-extracted with ethyl acetate (50 ml). The combined organic layers were re-extracted with conc. Sodium chloride solution, dried (MgSO4) and evaporated. The residue was purified by flash chromatography (20 g silica gel, 10% ethyl acetate in heptane) to yield a white solid (233 mg, 69%). MS (ISP): 289.1 ([M+H]+), 306.2 ([M+NH4]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181230B2
Source datasetuspto-grants-2015_11
ORD IDord-6aab78deb6fd45be876d214dd2156f5c
Source noteuspto-grants-2015_11