HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1-Diethylamino-6-m-methoxyphenylhex-2-yne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | CID 19593658 | HCID 19593658 | — |
| Reactant | 5-m-Methoxyphenylpent-1-yne | HCID 21221405 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Diethylamino-6-m-methoxyphenylhex-2-yne | HCID 21485597 | 736.2% |
Reaction Steps
Allow 5 -m-methoxyphenylpent-1-yne (8 g.) to stand for 12 hours at 70° C under nitrogen with water (2.5 cc), trioxan (0.5 g), 30% formalin (5.5 g), diethylamine (4 g), acetic acid (2.75 g), dioxan (25 cc) and cuprous chloride (0.13 g). Make the cooled solution alkaline with 10% aqueous sodium hydroxide and extract with ether; then extract the ether extract with 10% hydrochloric acid: wash the acid extract with ether, make alkaline with 10% aqueous sodium hydroxide, extract with ether, and then wash and dry the ether extract. Distil to obtain 1-diethylamino-6-m-methoxyphenylhex-2-yne (10.6 g. 88%), b.p. 130°-131° C/0.1 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002746 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-603744cb5b5147b2bb33041fd19e563d |
| Source note | uspto-grants-1977_01 |