HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 21485425, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Phenyl-1-pentyne | HCID 74573 | — |
| Reactant | CID 19593658 | HCID 19593658 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21485425 | HCID 21485425 | 886.9% |
Reaction Steps
Maintain 5-phenylpent-1-yne (20 g) for 12 hours at 70° under nitrogen with water (6.2 cc), trioxan (1.2 g), 30% formalin (13.8 g), diethylamine (10 g), acetic acid (6.9 g), dioxan (62 cc) and cuprous chloride (0.35 g). Make the cooled solution alkaline with sodium hydroxide. Extract with ether and extract the ether extract itself with hydrochloric acid. Make the purified aqueous hydrochloride solution thus obtained alkaline again and extract with ether. Dry, evaporate the ether extract and distil the residue to obtain 1-diethylamino-6-phenylhex-2-yne (27.1 g), b.p. 104°-106°/0.2 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002746 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-aa43cb0791e14b69b0bafcc88b8e1583 |
| Source note | uspto-grants-1977_01 |