HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270647Generated: October 27, 2026
Dichloromethane → 2-(2-Chloroethyl)-3-chloromethylthiophene
https://huagongshe.com/reaction/270647
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(3-Hydroxymethylthiophen-2-yl)ethanol | HCID 11182761 | — |
| Product | 2-(2-Chloroethyl)-3-chloromethylthiophene | HCID 69313345 | 27% |
Reaction Steps
3.0 g of the compound obtained in Example 2 was dissolved in 57 mL of dichloromethane, and the resulting solution was cooled to −3° C. To the solution, 6.1 g of diisopropylethylamine and 3.1 g of sulfuryl chloride were added, and the resulting mixture was stirred for 30 min at the same temperature and for an hour at room temperature. 20 mL of dichloromethane was added to the reaction solution, and the resulting mixture was washed twice with 40 mL portions of water. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to a silica gel column chromatography (eluent, n-hexane:ethyl acetate=10:1) to obtain 1.0 g (yield of 27%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449580B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-3a5d256c0c354ff4930801631dd178db |
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| Source note | uspto-grants-2008_11 |
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