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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028461Generated: October 26, 2026

Water → 2-(4-Isopropoxy-phenoxy)-5-tributylstannanyl-thiazole

https://huagongshe.com/reaction/1028461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTributyltin ChlorideHCID 15096—
Reactant2-(4-Isopropoxyphenoxy)-1,3-thiazoleHCID 67096922—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Isopropoxy-phenoxy)-5-tributylstannanyl-thiazoleHCID 1611075193%

Reaction Steps

To a solution of Example 1B (2.4 g, 0.01 mol) in dry tetrahydrofuran was added n-butyl lithium (4.4 mL, 2.5 M in hexane) at −78° C. drop wise. After stirring at this temperature for 1 h, tributyltin chloride (3.0 mL, 0.011 mol) was added slowly to the mixture. The brown solution was then stirred for 3 hours while warning up to room temperature. Water was added and the solution was extracted with ethyl acetate. The organic layer washed with saturated NH4Cl, brine, and then dried over magnesium sulfate. The solution was concentrated and the crude was purified on a silica gel flash column, eluting with 5-30% EtOAc in hexane, to give 4.85 g of the title compound (93% yield), 1H NMR (300 MHz, CDCl3) δ ppm 0.77-1.74 (m, 33 H) 4.40-4.63 (m, 1 H) 6.84-6.95 (m, 2 H) 7.12 (s, 1 H) 7.14-7.23 (m, 2 H). MS (ESI), m/z 526.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735595B2
Source datasetuspto-grants-2014_05
ORD IDord-744424346070415cb618dd3508734a82
Source noteuspto-grants-2014_05