HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5'-(2-Cyanovinyl)-1,3,3-trimethylspiro[indoline-2,3'-[3H]-naphtho[2,1-b][1,4]oxazine]
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (Cyanomethyl)triphenylphosphonium chloride | HCID 197040 | — |
| Reactant | 5'-Formyl-1,3,3-trimethylspiro[indoline-2,3'-[3H]-naphtho[2,1-b][1,4]oxazine] | HCID 15305689 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5'-(2-Cyanovinyl)-1,3,3-trimethylspiro[indoline-2,3'-[3H]-naphtho[2,1-b][1,4]oxazine] | HCID 53656886 | — |
Reaction Steps
1 ml of a 50% strength sodium hydroxide solution is added to a solution of 0.36 g (1 mmol) of the compound of Example 1 and of 0.34 g (1 mmol) of cyanomethyltriphenylphosphonium chloride in 3 ml of dichloromethane. The mixture is stirred at ambient temperature for 1 hour. 10 ml of water are then added and the aqueous phase is extracted with twice 10 ml of dichloromethane. The organic phase is washed, dried and evaporated. A purification is performed on a silica column (CH2Cl2 eluent).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06019914 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-a5f8570637924fefa3ca0013902b2091 |
| Source note | uspto-grants-2000_02 |