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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040028Generated: November 1, 2026

Nitrogen → 2-(tert-Butyl-dimethyl-silanyloxymethyl)-4-(2-methyl-[1,3]dioxolan-2-yl)-thiazole

https://huagongshe.com/reaction/2040028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 131729999HCID 131729999—
SolventEthylene GlycolHCID 174—
Product2-(tert-Butyl-dimethyl-silanyloxymethyl)-4-(2-methyl-[1,3]dioxolan-2-yl)-thiazoleHCID 131730001—

Reaction Conditions

Temperature95 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 1-[2-(tert-butyl-dimethyl-silanyloxymethyl)-thiazol-4-yl]-ethanone (1.77 g, 6.52 mmol) in ethylene glycol (7 mL) was treated with trimethylorthoformate (1.46 mL, 13.29 mmol) followed by LiBF4 (125 mg, 1.30 mmol). The reaction mixture was heated at 95° C. for 4 h. Sat. aq. Na2CO3 (5 mL) was added and the mixture was extracted with Et2O (2×20 mL). The org. extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1->3:1 hept-EA) gave the title compound as a brown oil. TLC:rf (1:1 hept-EA)=0.56. LC-MS-conditions 02: tR=1.11 min; [M+H]+=316.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580831B2
Source datasetuspto-grants-2013_11
ORD IDord-cbba2ff253e7416fa0205333a9ed624d
Source noteuspto-grants-2013_11