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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840597Generated: October 25, 2026

Methane, dichloromethoxy- → HCID 22620096, compound

https://huagongshe.com/reaction/840597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethane, dichloromethoxy-HCID 21004—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(4-Methoxyphenyl)-1,2,3-thiadiazoleHCID 2739349—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
ProductHCID 22620096HCID 22620096—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 0.99 grams (5.15 mmol) of 4-(4-methoxyphenyl)-1,2,3-thiadiazole (Maybridge Chemical Co.) in 23 mL of anhydrous methylene chloride (Ch2Cl2) cooled to 0° C., was treated with 2.3 mL (21.9 mmol) of titanium tetrachloride and stirred for 30 min. The red solution was treated with 0.97 mL (10.7 mmol) of α,α-dichloromethyl methyl ether and allowed to warm to room temperature overnight. The reaction mixture was then poured over 100 mL of saturated aqueous sodium bicarbonate (NaHCO3), the pH was adjusted to 7-8 with solid NaHCO3 and the solution was then extracted with CH2Cl2. The organic layer was dried with magnesium sulfate (MgSO4) and concentrated to a yellow solid. Chromatography on silica gel (20% EtOAc: 80% Hexane) gave the pure title compound as a light yellow solid, 0.35 g (31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369074B1
Source datasetuspto-grants-2002_04
ORD IDord-6e0277e160374ac7b4e9f9d85ae3a661
Source noteuspto-grants-2002_04