HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893266Generated: October 26, 2026
Acetic Acid → Dimethylaminomethylbenzylcyanide
https://huagongshe.com/reaction/893266
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(4-(Bromomethyl)phenyl)acetonitrile | HCID 14342076 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Dimethylaminomethylbenzylcyanide | HCID 415903 | — |
Reaction Steps
In a 1 liter round bottomed flask with condenser and thermometer 8.2 g of 4-bromomethylbenzylcyanide are dissolved in 453 ml methanol and cooled to +3° C. At this temperature 12.7 ml of 40% dimethylamine solution are added drop-by-drop. The solution is subsequently stirred for 1/4 hour at +5° C. and 2 hours at room temperature. The reaction sequence is controlled by means of thin-layer chromatography (0.57 ml of specimen+0.43 ml methanol: eluent n-butanol: acetic acid: water=4:1:1; v/v; 10 μl coating; HPTLC finished plated diatomaceous earth 60 F 254). Following removal of the volatile components is a rotary evaporator (20 torr, 40° C. bath temperature) the residue is absorbed in 20 ml 1N hydrochloric acid and extracted with a total of 150 ml of diethyl ether. The clear, aqueous phase is treated with 30 ml of 1N sodium hydroxide solution (ice cold) and extracted subsequently with 250 ml of diethyl ether. The organic phase is washed to neutrality with a saturated solution of common salt, dried with sodium sulfate and evaporated to dryness in a rotary evaporator (30° C. bath temperature, 20 torr).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05124326 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-370b8ce48f7f48c3bafaecdb5121d806 |
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| Source note | uspto-grants-1992_06 |
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