HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925257Generated: October 30, 2026
1,2-Ethanedithiol → HCID 86645389, compound
https://huagongshe.com/reaction/925257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67521261 | HCID 67521261 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86645389 | HCID 86645389 | 66.1% |
Reaction Steps
To a solution of acetic acid [3-(4-fluorophenyl)-3-oxo-propyl]ester (2.0 g, 9.52 mmol) in dry dichloromethane (40 ml) are added 1,2-ethanedithiol (1.79 g, 19.0 mmol) and boron trifluoride diethyl ether complex (0.68 g, 4.76 mmol) at 0° C. The resulting reaction mixture is stirred at RT for 16 h. After completion of reaction, the mixture is neutralized with 10M aqueous sodium hydroxide and extracted with DCM (3×100 ml). The combined organic layers are washed with water (100 ml), brine (100 ml), dried over anhydrous sodium sulfate and evaporated in vacuo to get the crude, which is purified by column chromatography (silica gel, 5% ethyl acetate/hexane) to yield acetic acid 2-[2-(4-fluorophenyl)-[1,3]dithiolan-2-yl]-ethyl ester (1.80 g, 6.29 mmol, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284286B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-ae9cee90a3d849b8b38d649f0af75e2b |
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| Source note | uspto-grants-2016_03 |
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