HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773Generated: October 26, 2026
Thionyl Chloride → 5-Oxotetrahydro-2-furancarbonyl chloride
https://huagongshe.com/reaction/1773
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Oxo-2-tetrahydrofurancarboxylic acid | HCID 251524 | — |
| Product | 5-Oxotetrahydro-2-furancarbonyl chloride | HCID 10844540 | — |
Reaction Steps
A mixture of 4.9 g of 5-oxotetrahydrofuran-2-carboxylic acid and 5.5 ml of thionyl chloride was subjected to reflux for 2 hours. Thionyl chloride was then distilled off under reduced pressure to leave 5-oxotetrahydrofuran-2-carbonyl chloride. This product was mixed with 5.0 g of 2-aminobenzophenone, 200 ml of ethyl acetate and 200 ml of a saturated aqueous solution of sodium hydrogencarbonate, which was stirred for one hour at room temperature. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluent, hexane:ethyl acetate=2:1) to give 2-(5-oxotetrahydrofuran-2-carbonyl)aminobenzophenone (6.5 g) as needles, m.p. 100° C.-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05726306 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-c2d7b50a1bd84d1e8cef8cf871d36f05 |
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| Source note | uspto-grants-1998_03 |
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