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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571825Generated: November 1, 2026

Ethyl Acetate → Tert-butyl 2-(4-amino-3-bromophenyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/571825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-bromobutanimideHCID 67184—
Reactanttert-Butyl 2-(4-aminophenyl)morpholine-4-carboxylateHCID 58315596—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 2-(4-amino-3-bromophenyl)morpholine-4-carboxylateHCID 71743185101.7%

Reaction Steps

To a stirred solution of tert-butyl (RS)-2-(4-aminophenyl)morpholine-4-carboxylate (3.07 g, CAS-1002726-96-6) in DMF (30 ml) was added NBS (1.96 g) and the mixture was stirred at room temperature for 15 min. The reaction mixture was then poured into EtOAc and extracted sequentially with water and with saturated brine. The organic layer was dried over Na2SO4 and then concentrated in vacuo to afford tert-butyl (RS)-2-(4-amino-3-bromophenyl)morpholine-4-carboxylate (4.0 g, quant.) as a light brown solid which was used in the next step without further purification. MS (ISP): 359.0 ([{81Br}M+H]+), 357.0 ([{79Br}M+H]+), 303.0 ([{81Br}M+H—C4H8]+), 301.0 ([{79Br}M+H—C4H8]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029370B2
Source datasetuspto-grants-2015_05
ORD IDord-5d1e57c5c3354146bac731a9303dac9d
Source noteuspto-grants-2015_05