HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395244Generated: November 3, 2026
Hexachloroethane → 5-Chlorothieno[2,3-d][1,2,3]thiadiazole-6-carboxylic acid
https://huagongshe.com/reaction/2395244
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexachloroethane | HCID 6214 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Thieno[2,3-d][1,2,3]thiadiazole-6-carboxylic acid | HCID 4715086 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chlorothieno[2,3-d][1,2,3]thiadiazole-6-carboxylic acid | HCID 1201389 | 98.7% |
Reaction Steps
79 ml (201.6 mmol) of n-butyllithium (1.6M in hexane) are added at -30° C., under nitrogen, to a solution of 20.4 g (201.6 mmol) of diusopropylamine in 200 ml of tetrahydrofuran (THF). After 20 minutes' stirring at -20° C., the LDA solution so prepared is added dropwise at -90° C., under nitrogen, by means of a capillary, to a suspension of 15.0 g (80.6 mmol) of thieno[2,3-d]1,2,3-thiadiazole-6-carboxylic acid in 150 ml of THF. After 90 minutes' stirring at -50° C., a solution of 42.0 g (177.2 mmol) of hexachloroethane in 70 ml of THF is added at -90° C. and the reaction mixture is heated to room temperature within a period of 2 hours. Then the reaction mixture is poured onto 2 litres of water, the aqueous phase is extracted with diethyl ether and acidified with concentrated hydrochloric acid, and the product is isolated by filtration. There are obtained 17.55 g of light-brown solid having a melting point of 255°-265° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05814629 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-6a3d7e26d5fb4e329c937cd0cd50e51a |
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| Source note | uspto-grants-1998_09 |
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