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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183516Generated: November 1, 2026

Dimethylformamide → HCID 69793206, compound

https://huagongshe.com/reaction/2183516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22473228HCID 22473228—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69793206HCID 6979320683.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of BuLi (23.6 mmol) in hexanes (1.6 M, 14.7 ml) was added to a stirred solution of 4-(tert-butyldimethylsilanyloxymethyl)-1-methyl-1H-[1,2,3]triazole (3.00 g, 13.2 mmol) in THF (50 ml) at −78° C. under N2. The resulting solution was stirred at −78° C. for 15 min, then warmed to −40° C. and recooled to −78° C. DMF (4.97 ml, 64.2 mmol) was added and the reaction was allowed to warm to room temperature. MeOH (50 ml) was added, followed by sodium borohydride (1.21 g, 32.1 mmol) and the reaction mixture was stirred at room temperature for 30 min. NH4Cl solution (50 ml) was added cautiously. The organic solvents were removed under reduced pressure, then 4N NaOH solution (50 ml) was added and the organics were extracted with CH2Cl2 (3×100 ml). The combined organic extracts were washed with NH4Cl solution (50 ml) and brine (50 ml), then dried and concentrated under reduced pressure. The crude residue was purified by column chromatography on silica using 3% MeOH/CH2Cl2 to yield the desired hydroxymethyltriazole (2.83 g, 83%). 1H NMR (360 MHz, CDCl3) δ 4.77 (2H, s), 4.62 (2H, d, J=5.9 Hz), 3.90 (3H, s), 0.78 (9H, s), 0.00 (6H,s). m/z (ES+) 258 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900209B2
Source datasetuspto-grants-2005_05
ORD IDord-58e2bacc877746329c5b3e34dab9549f
Source noteuspto-grants-2005_05