HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Butanamide, 4-chloro-N-(2,3,5,6,7,8-hexahydronaphtho[2,3-b]furan-7-yl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | HCID 19838440 | HCID 19838440 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | Butanamide, 4-chloro-N-(2,3,5,6,7,8-hexahydronaphtho[2,3-b]furan-7-yl)- | HCID 19838455 | — |
Reaction Steps
4.2 g of 4-chlorobutyryl chloride are added at room temperature to a mixture of 5 g of the compound of Example 2 and 4.2 g of triethylamine in 60 ml of benzene. After 1 hour at room temperature, the medium is diluted with water and filtered and the aqueous phase is extracted with benzene. The filtrate and the precipitate are combined and the benzene is evaporated off under vacuum. The dry residue is solidified in ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04885373 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-9218debab23b41eb9f63aad566202f4b |
| Source note | uspto-grants-1989_12 |