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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171535Generated: October 26, 2026

4-Acetylmorpholine → tert-Butyl [6-chloro-3-acetylpyridin-2-yl]carbamate

https://huagongshe.com/reaction/2171535

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AcetylmorpholineHCID 15543—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-butyl N-(6-chloropyridin-2-yl)carbamateHCID 11253185—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl [6-chloro-3-acetylpyridin-2-yl]carbamateHCID 59313093—

Reaction Conditions

Temperature-50 °C

Reaction Steps

0.65 g (2.9 mmol) of tert-butyl (6-chloropyridin-2-yl)carbamate (Example 105A) is introduced into 10 ml of THF and cooled to −50° C. 4.5 ml (7.2 mmol) of butyllithium (1.6 M) are added dropwise. After the dropwise addition is complete, the reaction is slowly warmed to −10° C. and kept at 0° C. for 2 h. It is then cooled to −40° C. again, and 740 mg (5.7 mmol) of N-acetylmorpholine dissolved in 4 ml of THF are added. The reaction solution is stirred at −40° C. for 1 h and then, at −40° C., poured into 1 l of ethyl acetate and 350 ml of ammonium chloride solution and extracted. The organic phase is separated off, dried over magnesium sulphate and concentrated in a rotary evaporator. The reaction mixture is chromatographed on silica gel (mobile phase cyclohexane/ethyl acetate 2:1). 218 mg (28% of theory) of the product are obtained as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051323B2
Source datasetuspto-grants-2015_06
ORD IDord-0ce0c2b21dd34b3b9f07fd4a04768a9a
Source noteuspto-grants-2015_06