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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044755Generated: November 1, 2026

Nitrogen → [5-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-2-yl]-methanol

https://huagongshe.com/reaction/1044755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant5-(2-Methyl-[1,3]dioxolan-2-yl)-thiazole-2-carbaldehydeHCID 86649488—
SolventMethanolHCID 887—
Product[5-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-2-yl]-methanolHCID 66819954—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), 5-(2-methyl-[1,3]dioxolan-2-yl)thiazole-2-carbaldehyde (5.12 g, 25.70 mmol) was dissolved in MeOH (60 mL). NaBH4 (1.26 g, 31.89 mmol) was added portionwise at 0° C. and the reaction mixture stirred at 0° C. for 1 h. Water was added and the mixture extracted with EA (3×). The combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure to give the title compound as an orange oil. TLC:rf (1:1 hept-EA)=0.31. LC-MS-conditions 02: tR=0.64 min; [M+H]+=202.52.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563714B2
Source datasetuspto-grants-2013_10
ORD IDord-fb31cfd042f04b1285153e949d2eb794
Source noteuspto-grants-2013_10