HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177236Generated: October 30, 2026
Sodium methanesulfinate → HCID 90418475, compound
https://huagongshe.com/reaction/2177236
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | HCID 90418750 | HCID 90418750 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 90418475 | HCID 90418475 | — |
Reaction Steps
Into a 50-mL round-bottom flask, was placed N,N-dimethylformamide (8 mL), CuI (391 mg, 2.05 mmol, 1.99 equiv), ethyl 3-(4-ethylphenyl)-5-iodo-1,2-thiazole-4-carboxylate (400 mg, 1.03 mmol, 1.00 equiv), sodium methanesulfinate (421.7 mg, 4.13 mmol, 4.00 equiv). The resulting solution was stirred for 16 h at 80° C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:20). The collected fractions were combined and concentrated under vacuum. This resulted in 170 mg (48%) of ethyl 3-(4-ethylphenyl)-5-methanesulfonyl-1,2-thiazole-4-carboxylate as a yellow solid. Mass spectrum (ESI, m/z): Calcd. for C15H17NO4S2, 340.1 (M+H). found 340.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067898B1 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-3e81f30873d24f18b0a50f2fff48dcd4 |
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| Source note | uspto-grants-2015_06 |
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