HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-2-butene → 2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | 2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehyde | HCID 21669817 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzoic acid | HCID 68717409 | 112.8% |
Reaction Steps
The above-obtained 2-(benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehyde (0.80 g, 2.3 mmol) was dissolved in tert-butyl alcohol (20 mL) and the obtained solution was added with 2-methyl-2-butene (10 mL, 94 mmol), sodium chlorite (2.0 g, 22 mmol), sodium dihydrogen phosphate (2.0 g, 17 mmol) and water (5 mL), followed by stirring at a room temperature for 10 hours. The reaction mixture was extracted with chloroform 3 times. The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate. Then the solvent was evaporated under reduced pressure to obtain 2-(benzyloxymethyl)-4,6-bis(methoxymethoxy)benzoic acid (0.94 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781485B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-acfebf0766b54e6a9f1d4344baad0be6 |
| Source note | uspto-grants-2010_08 |