HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3,3-Trimethyl-2-methyleneindoline → HCID 19388550, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3,3-Trimethyl-2-methyleneindoline | HCID 8351 | — |
| Reactant | HCID 22486123 | HCID 22486123 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19388550 | HCID 19388550 | 36.6% |
Reaction Steps
A solution of 4-(p-diethylaminophenyl)-1-nitroso-2 -hydroxynaphthalene (0.85 g; 0.0027 mol) and 1,3-dihydro-1,3,3-trimethyl-2-methyleneindoline (0.5 g; 0.0029 mol) in methanol (60 ml) under nitrogen, was heated under reflux for 24 hours. The solution was then evaporated and chromatographed over silica (1 part diethyl ether to 10 parts pet. ether) to afford 1,3-dihydro-1,3,3-trimethyl-6'-(p-diethylaminophenyl)spiro[2H-indole-2,3'-[3H]naphth[2,1-b][1,4]oxazine] (0.47 g; 36%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446151 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-1c034c0247c747388aad838b1bb9101b |
| Source note | uspto-grants-1995_08 |