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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103360Generated: November 2, 2026

Water → 8-(5-Methyl-1,3-thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/reaction/2103360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
Reactant8-(1,3-Thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-olHCID 57803329—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product8-(5-Methyl-1,3-thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-olHCID 5901744472.8%

Reaction Steps

A solution of n-butyllithium (5.70 mL of 1.6 M solution in hexane, 9.12 mmol) was added to 8-(1,3-thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-ol (1.00 g, 4.14 mmol) in THF (10 mL) at −78° C. with stirring under N2. After being stirred at −78° C. for 1 h, methyl iodide (0.71 mL, 9.12 mmol) was added to the lithiated compound solution via syringe at −78° C. The reaction mixture was allowed to warm to room temperature slowly and stirred overnight. Water and EtOAc were added. The aqueous layer was extracted with EtOAc (3×). The combined organic layers were washed with saturated NaCl, dried (MgSO4), concentrated and flash chromatographed using 20% EtOAc/hexane to give 0.77 g of the title compound in 71% yield. MS (EI) (M+H)+=256.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576089B2
Source datasetuspto-grants-2009_08
ORD IDord-880a07ec13154a7f8202d65f0ad629e7
Source noteuspto-grants-2009_08