HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459588Generated: October 26, 2026
Methane, dichloromethoxy- → HCID 22620096, compound
https://huagongshe.com/reaction/1459588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(4-Methoxyphenyl)-1,2,3-thiadiazole | HCID 2739349 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22620096 | HCID 22620096 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05854262 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-0ddb04c8a71c4be9a1b77ea52f0f425d |
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| Source note | uspto-grants-1998_12 |
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