HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → 3H-Indole, 2,3,3-trimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | 3-Methyl-2-butanone | HCID 11251 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3H-Indole, 2,3,3-trimethyl- | HCID 15427 | 97.5% |
Reaction Steps
226 g (2 mol) of phenylhy-drazine (95.7% pure) were initially introduced at 90° C. in a solution of 5 mol of sodium hydrogen sulphate in 1900 ml of water. 225 ml (2.1 mol) of methyl isopropyl ketone were added dropwise in the course of 30 min. The mixture was stirred for 3 h at 90° to 100° C. After cooling, the batch was neutralised and the organic phase was separated off and distilled. 299.3 g of 97.5% pure 2,3,3-trimethylindolenine were obtained Yield: 91.6% of the theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05179211 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-7cbbfff0c62b4ca99801784b33c152f2 |
| Source note | uspto-grants-1993_01 |