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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710810Generated: November 2, 2026

4-Methylmorpholine → HCID 86608958, compound

https://huagongshe.com/reaction/1710810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant2-Amino-3,6-dichlorobenzoic acidHCID 604542—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
SolventDimethylformamideHCID 6228—
ProductHCID 86608958HCID 8660895873%

Reaction Steps

N,O-dimethlyhydroxylamine hydrochloride (3.28 g, 33 mmol) and 2-amino-3,6-dichlorobenzoic acid (4.76 g, 22 mmol) were dissolved in DMF (110 ml). At r.t. under nitrogen and stirring, first N-methyl morpholine (10 g, 99 mmol) and then HBTU (12.5 g, 33 mmol) were added, and the reaction was stirred at r.t. overnight. The reaction was poured onto water and extracted twice with ethyl acetate. The organic layer was dried over sodium sulfate, filtered, and the solvent was evaporated. The residue was treated with heptane and little diethyl ether to yield 4 g of the product. The mother liquor was purified by column chromatography (silica gel, solvent gradient n-heptan/ethyl acetate=3/7) to give another batch of the title compound as an off-white solid (5.52 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790732B2
Source datasetuspto-grants-2010_09
ORD IDord-dac7d6924e074f33a0c29e03ad40b47d
Source noteuspto-grants-2010_09