HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-2-phenylethan-1-ol → HCID 20800573, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-2-phenylethan-1-ol | HCID 134797 | — |
| Reactant | 1(3H)-Isobenzofuranone,3-hydroxy-5-methyl-(9CI) | HCID 15190677 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20800573 | HCID 20800573 | — |
Reaction Steps
3-hydroxy-5-methyl-3H-isobenzofuran-1-one (4.66 g, 28.39 mmol) and H-phenylglycinol (3.89 g, 28.39 mmol) was taken up in dry toluene and heated to reflux under argon for 12 h. The water generated was collected in a Dean-Stark trap. The reaction mixture was cooled to room temp and poured into 1N HCl and the aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with saturated sodium bicarbonate, water, brine and dried over anhydrous magnesium sulfate. The solution was filtered and the solvent removed under reduced pressure. The product was isolated by flash chromatography. (4:1 hexane/ethyl acetate) Yield 5.20 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06906067B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-b039f3d468b94ca2833fa7bbc6e8228a |
| Source note | uspto-grants-2005_06 |