HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262431Generated: October 26, 2026
Sodium Chloride → 4-Hydroxybenzyl cyanide
https://huagongshe.com/reaction/262431
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Sodium 4-hydroxyphenylglycolate | HCID 23663713 | — |
| Product | 4-Hydroxybenzyl cyanide | HCID 26548 | — |
Reaction Steps
Sodium cyanide (25.0 g.) is added to a stirred suspension of anhydrous sodium p-hydroxymandelate (96 g. of 99% w/w material, the impurity being sodium chloride; prepared from 104 g. of monohydrate by azeotropic distillation with 500 ml. of xylene in a Dean and Stark apparatus) in N,N-dimethylformamide (100 ml.), and the mixture is heated at 135° C. for 1 hour and then cooled. Water (170 ml.) and formic acid (38 ml.) are added and the mixture is extracted twice with methyl isobutyl ketone (330 ml. and 170 ml. respectively). The combined extracts are washed twice with water (240 ml. and 180 ml. respectively) and then concentrated by evaporation. There is thus obtained a solution of p-hydroxybenzyl cyanide in methyl isobutyl ketone which is suitable for conversion to p-hydroxyphenylacetamide without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04154757 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-28aa4e4d450c4980b51e07ba96da11ab |
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| Source note | uspto-grants-1979_05 |
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