HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 1,4-Dihydronaphthalene-1-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1,4-Dihydronaphthalene-1-carboxylic acid | HCID 188523 | — |
| Product | 1,4-Dihydronaphthalene-1-carbonyl chloride | HCID 12604098 | — |
Reaction Steps
In an example of this reaction 1,4-dihydro-alpha-naphthoic acid is reacted with thionyl chloride at room temperature for 1-6 hours to obtain 1,4-dihydro-alpha-naphthoic chloride. This compound is then reacted with an amine of the formula (3) and triethylamine in ether solvent under reflux for 0.1-3 hours to obtain a compound of the formula (1a). Compounds of the formulae (1b) and (1c) may also be produced in the same manner as just described using 3,4-dihydro-alpha-naphthoic acid and 1,2,3,4-tetrahydro-alpha-naphthoic acid, respectively as starting materials.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04657581 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-64d60ab63ed24b22aecbf8b701cfadfd |
| Source note | uspto-grants-1987_04 |