HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714972Generated: October 27, 2026
Stannane, hydroxytrimethyl- → 2-Iodo-5-(4-methoxyphenyl)oxazole-4-carboxylic acid
https://huagongshe.com/reaction/714972
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannane, hydroxytrimethyl- | HCID 11217597 | — |
| Reactant | Ethyl 2-iodo-5-(4-methoxyphenyl)oxazole-4-carboxylate | HCID 68518841 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-Iodo-5-(4-methoxyphenyl)oxazole-4-carboxylic acid | HCID 68520872 | 100% |
Reaction Steps
To a solution of ethyl 2-iodo-5-(4-methoxyphenyl)oxazole-4-carboxylate (1.00 g, 2.7 mmol) in DCE (25 mL) was added trimethyl tin hydroxide (1.70 g, 9.4 mmol) and the resultant mixture stirred at 80° C. for 3 hours. Trimethyl tin hydroxide (0.24 g, 1.3 mmol) was then added and the reaction stirred at 80° C. overnight. The reaction was cooled to room temperature and extracted with DCM. The organic phase was washed with 1M aqueous HCl and brine, dried over MgSO4 and the solvent removed in vacuo to give 2-iodo-5-(4-methoxyphenyl)oxazole-4-carboxylic acid (0.92 g, 2.7 mmol, 99%) as a white solid which was used without further purification. 1H NMR (CDCl3) 3.88 (3H, s), 6.99 (2H, d), 8.13 (2H, d). LCMS (1) Rt: 1.03 min; m/z (ES+) 346.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187465B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-268a96153f2e4400a5c14199b77ec494 |
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| Source note | uspto-grants-2015_11 |
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