HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372028Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 10487636, compound
https://huagongshe.com/reaction/372028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10487636 | HCID 10487636 | — |
Reaction Steps
A mixture containing 50 milliliters (ml) of dimethylsulfoxide, 15 ml of water, 29 grams (g) of 2-chlorobenzaldehyde, 15 g of methylaminehydrochloride and 12.5 g of sodium cyanide is stirred at room temperature for approximately 76 hours. The reaction mixture is then diluted with water and extracted with benzene. The benzene extract is washed several times with water and then dried over potassium carbonate. Filtration and evaporation of the filtrate under reduced pressure yields crude 2-(2-chlorophenyl)-2-methylaminoacetonitrile. This material is dissolved in approximately 100 ml of ether and added to a solution of 13 g of lithium aluminum hydride in 300 ml of ether. The reaction temperature is kept between -10° and 5° C at first and is then allowed to warm to room temperature. After stirring for about 20 hours there is added cautiously and dropwise first 13 ml of water, then 13 ml of 15% sodium hydroxide and finally 20 ml of water. The mixture is stirred until the solid is nearly white and the solid is then removed by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04088771 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-de5feab0d2f443429c810c88307e8477 |
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| Source note | uspto-grants-1978_05 |
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