HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20233140, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 20233150 | HCID 20233150 | — |
| Reactant | 3-amino-2-chloro-6-ethyl-4H-1-benzothiopyran-4-one | HCID 20233152 | — |
| Reactant | HCID 73666279 | HCID 73666279 | — |
| Product | HCID 20233140 | HCID 20233140 | — |
Reaction Steps
In a manner analogous to that described in Example 1, starting from 4-ethylthiophenol there is obtained 3-(4-ethylphenylthio)-propionic acid, melting point 59°-60°, which is converted into 6-ethyl-2,3-dihydro-4H-1-benzothiopyran-4-one (red oil). This is converted into an oxime with isopentyl nitrite, and the resulting crude potassium salt of 6-ethyl-3-hydroxyimino-2,3-dihydro-4H-1-benzothiopyran-4-one is converted with concentrated hydrochloric acid into 3-amino-2-chloro-6-ethyl-4H-1-benzothiopyran-4-one, melting point 79°-81°. After hydrogenation there is obtained 3-amino-6-ethyl-4H-1-benzothiopyran-4-one having a melting point of 106°-107°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04614745 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-07a916fba8e84c9896463d2aeeb72752 |
| Source note | uspto-grants-1986_09 |