HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5-((3,3-Difluorocyclobutyl)methyl)-2,2-dimethyl-1,3-dioxane-4,6-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-[(3,3-Difluorocyclobutyl)carbonyl]-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 66878149 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-((3,3-Difluorocyclobutyl)methyl)-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 117690551 | 58% |
Reaction Steps
A solution of 5-(3,3-difluorocyclobutanecarbonyl)-2,2-dimethyl-1,3-dioxane-4,6-dione (15.0 g, 57.3 mmol) in THF (200 mL) was cooled to −5° C. and acetic acid (38 g, 0.63 mol) was added. The mixture was stirred for 5 min and sodium borohydride (6.5 g, 0.17 mol) was added in portions. The reaction mixture was stirred for 2 h at −5° C. and then poured into ice water (200 mL). The resulting mixture was extracted with EtOAc (300 mL×3). The organic extracts were combined, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by flash column chromatography on silica gel (dichloromethane/methanol=100:1 to 30:1) to afford 5-((3,3-difluorocyclobutyl)methyl)-2,2-dimethyl-1,3-dioxane-4,6-dione (8.2 g, 58% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434761B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-b8cad9fc48e84000a0a91b5ad3986e6e |
| Source note | uspto-grants-2016_09 |