Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605663Generated: October 30, 2026

Methyl 5-bromofuran-2-carboxylate → HCID 16110660, compound

https://huagongshe.com/reaction/605663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-bromofuran-2-carboxylateHCID 599633—
ReactantHCID 16110628HCID 16110628—
Reactant2-(1-(Tert-butyldimethylsilyloxy)-7-phenylheptyl)-5-(tributylstannyl)oxazoleHCID 67046048—
ProductHCID 16110660HCID 1611066099%

Reaction Steps

Methyl 5-(2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)oxazol-5-yl)furan-2-carboxylate. The title compound was prepared from 2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)-5-(tributylstannyl)oxazole (82 mg, 0.125 mmol) and methyl 5-bromofuran-2-carboxylate following General Procedure A. Flash chromatography (2-10% EtOAc/hexanes) yielded the title compound as a clear oil (62 mg, 99%): 1H NMR (CDCl3, 400 MHz) δ 7.42 (s, 1H), 7.29-7.25 (m, 3H), 7.19-7.16 (m, 3H), 6.70 (d, 1H, J=3.6 Hz), 4.83 (t, 1H, J=6.0 Hz), 3.92 (s, 3H), 2.60 (t, 2H, J=7.6 Hz), 1.96-1.85 (m, 2H), 1.71-1.57 (m, 2H), 1.40-1.33 (m, 6H), 0.90 (s, 9H), 0.10 (s, 3H), 0.00 (s, 3H); 13C NMR (CDCl3, 100 MHz) δ 163.8, 151.9, 149.1, 147.8, 147.5, 133.4, 133.2, 130.6, 129.3, 124.6, 113.6, 113.5, 73.6, 57.1, 41.3, 40.9, 36.4, 34.1, 30.7, 30.7, 30.1, 23.2, 0.0, −0.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915270B2
Source datasetuspto-grants-2011_03
ORD IDord-8ce82906b8b2466a9534236358470b78
Source noteuspto-grants-2011_03