HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4,4,4-trifluoroacetoacetate → NSC282112
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Reactant | 1H-Indol-6-amine, 2,3-dihydro-1,2,3,3-tetramethyl- | HCID 11816341 | — |
| Product | NSC282112 | HCID 323233 | — |
Reaction Steps
6-Amino-1,2,3,3-tetramethylindoline (6.9 g, 0.036 mole) was treated with 6.8 g of ethyl trifluoroacetoacetate. There was an immediate reaction with heat evolution and formation of a solid. The mixture was heated in an oil bath under a reflux condenser for 16 hrs at 135°-140° C., then for 1 hr at 145°-150° C. The cooled cake was broken up, triturated with 10 ml of diethyl ether, filtered and washed twice with cold ether; 7.7 g (69%). When recrystallized from 275 ml of 95% ethanol, the compound was obtained as felted, yellow needles; m.p. 248°-249° C., shrinking at 244° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04026898 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-70500e96a89742a0b6711bd8abab8905 |
| Source note | uspto-grants-1977_05 |