HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine → HCID 53881320, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine | HCID 547712 | — |
| Reactant | 6-Phenyl-1,3-dihydro-indol-2-one | HCID 10536384 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53881320 | HCID 53881320 | 75% |
Reaction Steps
6-Phenyloxindole (0.053 mg, 0.25 mmol) and dimethylformamide di-t-butylacetal (0.08 mL, 0.32 mmol) were combined and dissolved in DMF. The reaction mixture was stirred at room temperature for 4 hours. The volatiles were removed in vacuo and the resulting residue was triturated with diethyl ether. The solids were collected by filtration (50 mg, 75% yield). ). 1H NMR 400 MHz (DMSO-d6) mixture of E and Z isomers: δ10.09 (s, 1H); 10.02 (s, 1H); 7.59-7.51 (m, 4H); 7.45-7.22 (m, 10H); 7.10-7.05 (m, 2H); 6.98 (s, 1H); 6.91 (s, 1H); 3.29 (s, 12H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06369086B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-4b4814401bd74388909f851ec7645917 |
| Source note | uspto-grants-2002_04 |