HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diketene → HCID 23346106, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diketene | HCID 12661 | — |
| Reactant | 1,1,1,3,3,3-hexafluoro-2-(2-methyl-2,3-dihydro-1H-indol-5-yl)-propan-2-ol | HCID 23346126 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23346106 | HCID 23346106 | 74.4% |
Reaction Steps
To a stirred solution of 6.0 g (0.02 mole) of α,α-bis(trifluoromethyl)-2,3-dihydro-2-methyl-1H-indole-5-methanol in 50 ml of anhydrous tetrahydrofuran is added 1.9 g (0.022 mole) of diketene. After 16 hours at room temperature, the solution is refluxed for one hour. The solvent is evaporated, and the residue is recrystallized from dibutyl ether to give 5.7 g (74%) of α,α-bis(trifluoromethyl)-1-(1,3-dioxobutyl)-2,3-dihydro-2-methyl-1H-indole-5-methanol, m.p. 118°-119°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04218448 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-a134ac6b6aad4716a29c1ca2a801f9cd |
| Source note | uspto-grants-1980_08 |