HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 15222348, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 6,6,6-trifluorohexylacetoacetate | HCID 15222347 | — |
| Product | HCID 15222348 | HCID 15222348 | — |
Reaction Steps
Ethyl 6,6,6-trifluorohexylacetoacetate was added at -35° C. to a solution of sodium (50 moles, 1.15 g) in 150 ml ethanol and stirred for 15 minutes. N-Bromosuccinimide (50 moles, 8.9 g) was added. The solution was allowed to warm to room temperature and stirred for 2.5 hours. The mixture was poured into water. The intermediate was extracted with hexane. The solvent was removed. The oil was chromatographed over silica gel eluted with hexane to yield 13.6 g of ethyl 2-bromo-8,8,8-trifluorooctanoate. (MS).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05401851 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-7e690287f1fa4b1fbd130dba3e7beaed |
| Source note | uspto-grants-1995_03 |