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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82830Generated: October 29, 2026

Nitrogen → (2-(Methoxymethyl)thiazol-5-yl)methanol

https://huagongshe.com/reaction/82830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]-2-(methoxymethyl)thiazoleHCID 86698206—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(2-(Methoxymethyl)thiazol-5-yl)methanolHCID 64980908—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 5-(((tert-butyldimethylsilyl)oxy)methyl)-2-(methoxymethyl)thiazole (721 mg, 2.64 mmol) in THF (20 mL) was treated at 0° C. with TBAF (5.30 mL of a 1M solution in THF, 5.30 mmol) and the resulting mixture was stirred for 45 min at 0° C. The reaction mixture was diluted with EA, washed with sat. aq. NH4Cl and brine, dried over Na2SO4, filtered and the solvent was removed under reduced pressure. Purification of the residue by FC (1:9 hept-EA) gave the title compound as a colorless oil: TLC: rf (1:9 hept-EA)=0.27. LC-MS-conditions 07: tR=0.41 min, [M+H]+=160.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846733B2
Source datasetuspto-grants-2014_09
ORD IDord-46d02a1dee8e4f369dfdb16fb9e08382
Source noteuspto-grants-2014_09