HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29241Generated: October 29, 2026
Thionyl Chloride → HCID 59788880, compound
https://huagongshe.com/reaction/29241
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(2,4-Dichloro-benzoyl)-6-m-tolyl-benzofuran-3-carboxylic acid amide | HCID 59788940 | — |
| Product | HCID 59788880 | HCID 59788880 | 13.2% |
Reaction Steps
A mixture of 2-(2,4-Dichloro-benzoyl)-6-m-tolyl-benzofuran-3-carboxylic acid amide from Example 2 step 7 (46.2 mg, 0.11 mmol) and SOCl2 (3 mL) was heated at 80° C. for 15 h. The reaction was cooled down to rt and the solvent was removed under reduced pressure. The residue was purified by pre-HPLC to afford a yellow solid (5.9 mg, 13%) as product. 1H-NMR (CDCl3): δ 7.88 (d, J=8.3 Hz, 1H), 7.79 (s, 1H), 7.73 (dd, J=1.5, 8.3 Hz, 1H), 7.54 (d, J=1.5 Hz, 1H), 7.52 (d, J=8.3 Hz, 1H), 7.4 (dd, J=1.5, 8.3 Hz, 1H), 7.41 (m, 2H), 7.36 (t, 1H), 7.23 (d, J=8.3 Hz, 1H), 2.42 (s, 3H); LC-MS (MH+=406/408).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07420066B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-d94c1ec1227f44beae2c8eb8028e8dca |
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| Source note | uspto-grants-2008_09 |
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