HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20528325, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzoin | HCID 8400 | — |
| Reactant | Veratraldehyde | HCID 8419 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | 1,3-Diazepane-2-thione | HCID 736589 | — |
| Reactant | 3,4-Dimethoxy-2'-fluorobenzoin | HCID 20528310 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20528325 | HCID 20528325 | — |
Reaction Steps
A mixture consisting of 16.6 g. of veratraldehyde, 12.5 g. of o-fluorobenzaldehyde, 8 g. of potassium cyanide, and 100 ml of 65% ethanol is reacted as described in Example 20, yielding 12.5 g. of 3,4-dimethoxy-2'-fluorobenzoin, m.p. 126°-128° C. A 5.8 g. portion of the benzoin derivative is converted to its methanesulfonate ester by the procedure of Example 20, giving 6.7 g. of the ester melting at 111°-113° C. 2.58 g. of the methanesulfonate ester, 0.91 g. of hexahydro-2H-1,3-diazepin-2-thione, and 55 ml. of acetone are mixed and left at room temperature for three days. 7 ml. of 2 N ethanolic hydrogen chloride are added, yielding 2.2 g. of the title compound, melting at 192°-194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04344954 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-2c17cee5591046558cc1b46ca1a3b269 |
| Source note | uspto-grants-1982_08 |