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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389739Generated: October 28, 2026

Stannane, hydroxytrimethyl- → 2-Iodo-5-(4-methoxyphenyl)oxazole-4-carboxylic acid

https://huagongshe.com/reaction/389739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, hydroxytrimethyl-HCID 11217597—
ReactantEthyl 2-iodo-5-(4-methoxyphenyl)oxazole-4-carboxylateHCID 68518841—
Solvent1,2-DichloroethaneHCID 11—
Product2-Iodo-5-(4-methoxyphenyl)oxazole-4-carboxylic acidHCID 68520872100%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378095B2
Source datasetuspto-grants-2013_02
ORD IDord-f3c362f2d0004c1fa1859baecbe9ff1c
Source noteuspto-grants-2013_02