HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 21412092, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Reactant | HCID 21412120 | HCID 21412120 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21412092 | HCID 21412092 | — |
Reaction Steps
3-Dimethylsulfamoyl-5H-dibenzo[a,d]cyclohepten-5-one (6.9 g., 0.022 mole) and 100 ml. of absolute methanol are stirred and heated to refluxing. A solution of 1.6 g. (0.0296 mole) of potassium borohydride in 12 ml. of water containing 1 pellet of potassium hydroxide is added dropwise at a rate such that reflux is maintained without external heating. After another 11/2 hours at reflux, the solution is evaporated to dryness under reduced pressure. The residual white solid is suspended in water, collected, and crystallized from 95% ethanol. The yield of 3-dimethylsulfamoyl-5H-dibenzo[a,d]cyclohepten-5-ol is 6.05 g. (87%), m.p. 150°-152°C. The melting point is unchanged by further recrystallization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03981917 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-aca41dc8c2e1452387cdb290b3250e5a |
| Source note | uspto-grants-1976_09 |