HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364124Generated: October 30, 2026
Trifluoroacetic acid → HCID 20154010, compound
https://huagongshe.com/reaction/364124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 10630640 | HCID 10630640 | — |
| Reactant | HCID 20154025 | HCID 20154025 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20154010 | HCID 20154010 | — |
Reaction Steps
The starting material is prepared as follows: A mixture of 7.5 g 6-methoxythiochroman-3-one [J. Org. Chem. 34, 1566 (1969)], 5.8 g of methyl 3-(propylamino)-propionate and 0.8 ml of trifluoroacetic acid in 80 ml of toluene is heated under reflux for 22 hours in a Dean Stark apparatus. Additional 0.8 ml portions of trifluoroacetic acid are added after 2, 5, and 16 hours. The solvent is removed, the residue is taken up in ether and the product is extracted with 3N hydrochlorid acid. After neutralization the aqueous layers are extracted with ethyl acetate, the organic layer is dried and the solvent is removed. The product is crystallized from a small volume of methanol to afford 9-methoxy-4-propyl-1,2,3,5-tetrahydro-4H-[1]-benzothiopyrano[3,4-b]pyridin-1-one, m.p. 108°-110°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04604397 |
|---|
| Source dataset | uspto-grants-1986_08 |
|---|
| ORD ID | ord-f3fe596c13e54c37bfeeb77c9a2c4e9f |
|---|
| Source note | uspto-grants-1986_08 |
|---|