HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20434118, compound → HCID 13365124, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20434118 | HCID 20434118 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13365124 | HCID 13365124 | 81% |
Reaction Steps
A mixture of 1.5 g of α-[(α-methyl-4-methoxyphenethylamino)methyl]-2-benzyloxybenzylalcohol oxalate [the diastereoisomer of M.p. 138°-139° C. (decomp.)], 0.3 g of 10% palladium-carbon and 30 ml of 90% aqueous ethanol is treated in the same manner as described in Example 1-(4-a). The crude product is recrystallized from ethanol in the presence of 300 mg of oxalic acid, and crystalline precipitates are collected by filtration. 0.76 g of α-[(α-methyl-4-methoxyphenethylamino)methyl]-2-hydroxybenzylalcohol 3/2 oxalate [the diastereoisomer of M.p. 175°-176° C. (decomp.)] is thereby obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04490392 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-8eb742357f3742ee807c76e8a7ec65fb |
| Source note | uspto-grants-1984_12 |