HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4-Benzyloxy-1-methoxymethyl-isoquinoline-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Benzyloxy-1-methoxymethyl-isoquinoline-3-carboxylic acid benzyl ester | HCID 66713169 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Benzyloxy-1-methoxymethyl-isoquinoline-3-carboxylic acid | HCID 66712892 | 90.2% |
Reaction Steps
A mixture of 4-Benzyloxy-1-methoxymethyl-isoquinoline-3-carboxylic acid benzyl ester (198 mg, 0.48 mmol), KOH (325 mg, 5 mmol) and EtOH (10 ml) was stirred at ambient temperature for 18 h before the solvent was evaporated in vacuo. To the residue was added water (25 ml) and the mixture was washed with Et2O (2×25 ml). Then the solution was acidified by addition of aqueous 6N HCl and extracted with EtOAc (25 ml). The organic phase was dried over MgSO4 and concentrated in vacuo to give the title compound as a yellow oil (140 mg); MS-(+)-ion: M+1=324.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09339527B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-0266c949d36f4347a88127c7403fbf0c |
| Source note | uspto-grants-2016_05 |