HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 12893929, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Cyanate | HCID 517096 | — |
| Reactant | 1-[2-(Hydroxymethyl)bicyclo[2.2.1]hept-5-en-2-yl]ethan-1-one | HCID 12893798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12893929 | HCID 12893929 | 54.7% |
Reaction Steps
52 g (0.8 mole) of sodium cyanate, followed dropwise by 95.8 g (0.84 mole) of trifluoroacetic acid, are added to a solution of 66.4 g (0.4 mole) of 2-hydroxymethylnorborn-5-en-2-yl methyl ketone in 120 ml of methylene chloride at 20° C., with slow stirring. The mixture is then stirred for 5 hours at room temperature, after which it is diluted with water. It is then repeatedly extracted with methylene chloride and the organic phases are combined and dried over sodium sulfate. After distilling off the solvent, a crystalline residue (83.1 g=99%) is obtained, and this is recrystallized from ethyl acetate. 45.8 g of 2-carbamyloxymethylnorborn-5-en-2-yl methyl ketone, of melting point 118°-119° C., are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04335138 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-d55f6f0518734c199302d9ccb75a867e |
| Source note | uspto-grants-1982_06 |