HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374866Generated: October 30, 2026
Trifluoroacetic acid → HCID 15284123, compound
https://huagongshe.com/reaction/374866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 15284122 | HCID 15284122 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15284123 | HCID 15284123 | — |
Reaction Steps
In to a cold (-78° C.) solution of tert-butyl acetate (2.7 mL, 19.96 mmol) in THF (35 mL) was added lithium bis(trimethylsilyl)amide solution (1 .0M, 21.62 mL, 21.62 mmol). After stirring for 2 hours a solution of trifluoromethanesulfonic acid 2-(5-bromo-naphthalen-2-ylmethyl)-3-oxo-cyclohex-1-enyl ester (7.7 g, 16.63 mmol) in THF (15 mL) was added dropwise. The mixture was stirred for 1 hour, quenched with aqueous NH4Cl, poured in to H2O and extracted with EtOAc, The organic extracts were dried over MgSO4. Evaporation gave a yellow oil residue which was taken up in methylene chloride (100 mL) and treated with trifluoroacetic acid (10 mL). The mixture was stirred for 5 hours and then the volatiles were removed in vacuo. The residue was purified by flash chromatography on acidic silica gel (eluting solvent hexane/EtOAc 1/1) to give a yellow solid (4.1 g, 66% yield, m.p 56°-58 ° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05482968 |
|---|
| Source dataset | uspto-grants-1996_01 |
|---|
| ORD ID | ord-6b7a9bf3143541c6b81ce48001596f03 |
|---|
| Source note | uspto-grants-1996_01 |
|---|