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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719235Generated: November 2, 2026

HCID 20267946, compound → 3-[(Chloromethoxy)methyl]-1,2,5-thiadiazole

https://huagongshe.com/reaction/1719235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20267946HCID 20267946—
ReactantHCID 86740280HCID 86740280—
SolventDichloromethaneHCID 6344—
Product3-[(Chloromethoxy)methyl]-1,2,5-thiadiazoleHCID 20267933—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(Chloromethyloxymethyl)-1,2,5-thiadiazole Sulfuryl chloride (0.24 mmol) in dry dichloromethane (0.5 ml) was added dropwise over a period of 3 minutes at 0° C. to a solution of 3-(Methylthiomethyloxy)methyl-1,2,5-thiadiazole (0.24 mmol) in dry dichloromethane (1.5 ml). The mixture was stirred at 0° C. for 5 minutes and at room temperature for 10 minutes before the solution was evaporated at reduced pressure. The crude product (30 mg, 75%) was used for alkylation in Example 9 without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539324
Source datasetuspto-grants-1985_09
ORD IDord-083b88cce4a9445282ab2e9db73c84c2
Source noteuspto-grants-1985_09