Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866083Generated: November 3, 2026

Methoxyacetyl chloride → HCID 178494705, compound

https://huagongshe.com/reaction/1866083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetyl chlorideHCID 96623—
ReactantThiosemicarbazideHCID 2723789—
SolventPyridineHCID 1049—
ProductHCID 178494705HCID 17849470533%

Reaction Steps

Methoxyacetyl chloride (2.82 g; 0.023 mol) was added to a solution (15 ml) of 2.09 g (0.0230 mol) of thiosemicarbazide in pyridine followed by stirring for a whole day and night at room temperature. The reaction solution was concentrated and 10 ml of methanol and 8 ml of a 25 wt % methanolic solution of sodium methoxide were added thereto followed by heating to reflux for a whole day and night. After cooling to room temperature, the solvent was evaporated and concentrated hydrochloric acid was added thereto to acidify. The solid separated out therefrom was filtered, washed with distilled water and dried to give 1.0 g (yield: 33%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629362B2
Source datasetuspto-grants-2009_12
ORD IDord-d2d494cd16b64ec68a435dd371cca579
Source noteuspto-grants-2009_12