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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710236Generated: October 29, 2026

N-Methoxy-N-methylacetamide → tert-Butyl 2-(4-acetylphenyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/710236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylacetamideHCID 537505—
ReactantTert-butyl 2-(4-bromophenyl)morpholine-4-carboxylateHCID 58097878—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 2-(4-acetylphenyl)morpholine-4-carboxylateHCID 89689432—

Reaction Conditions

Temperature-78 °C

Reaction Steps

tert-Butyl 2-(4-bromophenyl)morpholine-4-carboxylate (750 mg, 2.19 mmol, CAS 1131220-82-0) in THF (6 ml) was cooled to −78° C., treated dropwise with n-butyllithium (2.05 ml, 3.29 mmol, 1.6 M solution in hexane) and stirred 1 h at −78° C. N-Methoxy-N-methylacetamide (226 mg, 2.19 mmol) was added and the mixture was stirred for 1 h at −78° C., and then allowed to warm up to −5° C. The reaction mixture was quenched by addition of saturated ammonium chloride solution (4 ml) and water (4 ml) and the resulting mixture was partitioned between water and ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181230B2
Source datasetuspto-grants-2015_11
ORD IDord-e8f36dce21474d75927ad3cec26f6f15
Source noteuspto-grants-2015_11