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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295222Generated: November 2, 2026

Ammonium Chloride → 3-benzyloxy-1-methyl-1H-pyrazol-4-ylacetonitrile

https://huagongshe.com/reaction/1295222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant3-(benzyloxy)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 22930723—
ReactantPotassium tert-butoxideHCID 23665647—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-benzyloxy-1-methyl-1H-pyrazol-4-ylacetonitrileHCID 6942871982%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixture of potassium t-butoxide (2.24 g) and dimethoxyethane (10 ml) was added a solution of p-toluenesulfonylmethyl isocyanide (2.05 g) in dimethoxyethane (10 ml) and the mixture was stirred at −78° C. for 5 min. Then a solution of 3-benzyloxy-1-methyl-1H-pyrazole-4-carbaldehyde (2.16 g) in dimethoxyethane (10 ml) was added. After stirring at said temperature for 1 hr, the mixture was stirred for 1 hr. while raising the temperature to room temperature. To the obtained mixture was added methanol (380 ml), and the mixture was refluxed for 1 hr. After cooling, the reaction solution was poured into saturated aqueous ammonium chloride solution and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and 3-benzyloxy-1-methyl-1H-pyrazol-4-ylacetonitrile (1.86 g, yield 82%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (1:2, volume ratio).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-eff547795e414cdd9b7878b9e4443ea7
Source noteuspto-grants-2007_07