HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diketene → (R)-1-trichloromethyl-3-methyl-2-butenyl acetoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diketene | HCID 12661 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (2R)-1,1,1-trichloro-4-methyl-3-penten-2-ol | HCID 11095708 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-1-trichloromethyl-3-methyl-2-butenyl acetoacetate | HCID 12525204 | 85.2% |
Reaction Steps
A mixture of (2R)-1,1,1-trichloro-4-methyl-3-penten-2-ol (1.50 g., 7.35 mmole) from Example IA.1.(a) and a trace of sodium acetate was treated under nitrogen at 100° with freshly distilled diketene (0.70 g, 8.36 mmole) added dropwise over 1 hr. After stirring and heating an additional hour at 80°-83°, the cooled reaction mixture was diluted with 3 ml of CH2Cl2 and chromatographed on 8 (20×20 cm) preparative tlc plates, developed in CH2Cl2. Isolation and extraction afforded (1R)-3-methyl-1-trichloromethyl-2-butenyl acetoacetate (1.80 g, 85% isolated yield) as a pale yellow oil; [α]D31 =+21.1° (hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04283341 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-17ec5da1e1364267bbfbe124b47cae0c |
| Source note | uspto-grants-1981_08 |