HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfamic Acid → 2-[1,1-dimethyl-2-((R)-2-trifluoromethyloxiranyl)ethyl]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | 2-[1,1-dimethyl-2-((R)-2-trifluoromethyloxiranyl)ethyl]benzaldehyde | HCID 58026157 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-[1,1-dimethyl-2-((R)-2-trifluoromethyloxiranyl)ethyl]benzoic acid | HCID 49821360 | 85% |
Reaction Steps
To a stirred, ice-cooled, acetonitrile (250 mL) solution of 2-[1,1-dimethyl-2-((R)-2-trifluoromethyloxiranyl)ethyl]benzaldehyde (20 g, 73.5 mmol) was added a solution of sodium chlorite (7.4 g, 73.5 mmol in 100 mL water) followed immediately by a solution of sulfamic acid (7.13 g, 73.5 mmol in 100 mL water). After 30 minutes, the ice-cooled reaction mixture was treated with 500 mL of brine and extracted with three 300 mL portions of ethyl acetate. The combined extracts were washed with brine, dried over anhydrous sodium sulfate, and the solvent evaporated in vacuo to give 2-[1,1-dimethyl-2-((R)-2-trifluoromethyloxiranyl)ethyl]benzoic acid as a colorless thick oil (18 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268859B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-405bd9893fd24589ba48376106685b36 |
| Source note | uspto-grants-2012_09 |