HuagongsheHuagongshe Chemistry Print Report · For research reference only
Urea → 3-Cyano-8-fluorodibenzo[b,f]thiepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | 8-Amino-3-cyanodibenzo[b,f]thiepin | HCID 13151883 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Cyano-8-fluorodibenzo[b,f]thiepine | HCID 13490387 | — |
Reaction Steps
Suspend 6 gm. of the 3-cyano-8-aminodibenzo[b,f]thiepine from Example 18, Step 1, in 15 ml. of 50% fluoboric acid (HBF4) and 15 ml. of water. Cool the mixture to 3°-5° C. and slowly add 18 ml. of 10% sodium nitrite. Stir in the cold for 4 hours and add urea to destroy the excess sodium nitrite. Separate the solids by filtration and wash with cold 5% fluoboric acid followed by cold water and then ether. Air dry. Suspend the diazonium fluoroborate in 300 ml. of xylene and reflux for 2 hours with stirring. Filter and evaporate the filtrate to dryness. Triturate with ether to obtain the title product (m.p., 146°-148° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536507 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-2c6b36c3bda143b8ba8a2e7f27ec5284 |
| Source note | uspto-grants-1985_08 |