HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl chlorophosphate → HCID 178490123, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 5-[4-(Benzyloxy)-3-methoxyphenyl]penta-2,4-dienoic acid | HCID 54225043 | — |
| Reactant | HCID 178461400 | HCID 178461400 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178490123 | HCID 178490123 | — |
Reaction Steps
Using 4g of 4-(4-benzyloxy-3-methoxyphenyl)-l,3-butadiene-1-carboxylic acid, 3 ml of diethyl chlorophosphate, 3.5 ml of triethylamine, 150 ml of methylene chloride, 2.2 g of trans-4-methylcyclohexylammonium chloride, and 0.5 g of -dimethylaminopyridine, a reaction similar to that conducted in Example 81 was carried out. As a result, 3.62 g of N-(trans-4-methylcyclohexyl)-4-(4-benzyloxy-3-methoxyphenyl)-1,3-butadiene-l-carboxamide (a compound of the present invention) was obtained as a pale yellowhish brown oil, which had the following physiochemical properties:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05344845 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-158ab7a71a614632b9a8a73768063b90 |
| Source note | uspto-grants-1994_09 |