HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 2,2-Dimethyl-4-benzyloxycarbonylbutyric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,2-Dimethylglutaric acid | HCID 12681 | — |
| Reactant | Dihydro-3,3-dimethyl-2H-pyran-2,6(3H)-dione | HCID 76247 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Dimethyl-4-benzyloxycarbonylbutyric acid | HCID 19080045 | 73.6% |
Reaction Steps
To a mixture of 3 g (0.021 mol) of 2.2-dimethylglutaric anhydride, 2.0 ml (0.019 mol) of benzyl alcohol in 10 ml of CH2Cl2 was added 100 mg of DMAP and 3.4 ml of pyridine. The resulting solution was stired at room temperature for 4 h. After additional 2.2-dimethyl-glutaric acid (0.7 g, 4.9 mmol) was added, the mixture continued to be stirred overnight, then poured into 0.5M H2SO4 (aq.) solution and extracted with CH2Cl2. The organic layer was washed with brine, dried over Na2SO4 and filtered. Concentration followed by purification by flash chromatography on silica gel using EtOAc/hexane (1:1) as the irrigant gave 3.5 g of desired product in 66% yield and 1.2 g of isomer in 23% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05767256 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-42e4ecca3cde4cb382cfced4daddbcd4 |
| Source note | uspto-grants-1998_06 |