HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 67745337, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 67745330 | HCID 67745330 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67745337 | HCID 67745337 | 83.3% |
Reaction Steps
3.95 cm3 of acetic anhydride are added to a suspension of 2.7 g of 4,4-diphenyltetrahydrothiapyran 1-oxide in 30 cm3 of anhydrous toluene. The mixture is refluxed for 20 hours and concentrated to dryness at 60° C. under reduced pressure (2.7 kPa and then 0.13 kPa). The oily residue is crystallized from diisopropyl oxide, the crystals are drained and dried. 2.1 g of 3,4-dihydro-4,4-diphenyl-2H-thiapyran are obtained in the form of white crystals; melting point 78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05484942 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-d4e360728783413687354eb3f0b50cfe |
| Source note | uspto-grants-1996_01 |