HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiochroman-4-one → 3,4-Dihydro-2H-1-benzothiopyran-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiochroman-4-one | HCID 19048 | — |
| Reactant | HCID 20163643 | HCID 20163643 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 3,4-Dihydro-2H-1-benzothiopyran-4-ol | HCID 375102 | — |
Reaction Steps
Reduction of thiochroman-4-one with lithium aluminum hydride by the method of Preparation O, Part (iii), affords thiochroman-4-ol in like manner. This is taken up in acetic acid containing a molar excess of acetic anhydride, the mixture heated at reflux for three hours, cooled, ethanol added to quench the excess anhydride and the mixture hydrogenated by the method of Example 11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04703052 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-0ed15ad592464ddb8da349c6de037d0b |
| Source note | uspto-grants-1987_10 |