HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 1-Cyanoethyl 4-(hexadecylamino)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Hexadecylaminobenzoyl chloride hydrochloride | HCID 13255322 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Cyanoethyl 4-(hexadecylamino)benzoate | HCID 23457872 | — |
Reaction Steps
A mixture of 1 g. (16.1 m moles) potassium cyanide, 5 ml. diisopropylethylamine and 800 mg. (18.1 m moles) acetaldehyde in 50 ml. tetrahydrofuran is stirred for 2 hours at room temperature. To this solution is added 6.7 g. (16.1 m moles) 4-(hexadecylamino)benzoyl chloride hydrochloride in 50 ml. tetrahydrofuran. After stirring for an additional 2 hours, the solution is diluted with 100 ml. water and extracted with ether. After drying with magnesium sulfate, the ether is evaporated and the residue is crystallized from acetonitrile to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04254138 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-6bcecfc534544f4aa1add9d0d6c07ded |
| Source note | uspto-grants-1981_03 |