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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | 3-(benzyloxy)-1-methyl-1H-pyrazole-4-carbaldehyde | HCID 22930723 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 3-benzyloxy-1-methyl-1H-pyrazol-4-ylacetonitrile | HCID 69428719 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241785B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-eff547795e414cdd9b7878b9e4443ea7 |
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| Source note | uspto-grants-2007_07 |
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