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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765037Generated: October 25, 2026

Morpholine → 5,5-Dichloro-1-morpholinopent-4-ene-1,3-dione

https://huagongshe.com/reaction/1765037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-4-(2,2,2-trichloroethyl)oxetan-2-oneHCID 6605260—
SolventDichloromethaneHCID 6344—
Solventtert-Butyl methyl etherHCID 15413—
Product5,5-Dichloro-1-morpholinopent-4-ene-1,3-dioneHCID 660526172,927.5%

Reaction Conditions

Temperature15 °C

Reaction Steps

Two separate solutions of 4-Chloro-4-(2,2,2-trichloro-ethyl)-oxetan-2-one (62.5 g, 0.26 mmol) and morpholine (24.0 g, 0.28 mol) in dichloromethane (120 ml) were added simultaneously to a mixture of NaHCO3 (44.0 g, 0.52 mol) in dry dichloromethane (300 ml). The reaction was maintained at 15° C. over 140 min with stirring. The reaction was filtered, washed with dichloromethane (3×100 ml) and the combined organic layers were concentrated in vacuo to a slurry which was then passed through a short silica pad, and further washed with dichloromethane (4×100 ml). The combined organic layers were concentrated in vacuo, suspended in hexane (400 ml) and stirred for 1 h, filtered and dried to give a cream solid. The solid was suspended in tert-butyl methyl ether (100 ml), stirred for 15 min, filtered, washed with butyl methyl ether and dried to give the desired compound as a white powder (47.8 g, 72%). m/z (LC-MS, ESP): 252 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226918B2
Source datasetuspto-grants-2007_06
ORD IDord-176d1684d67c4369a0dacaacdf0116ff
Source noteuspto-grants-2007_06