HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2,3-Dihydro-1H-isoindole-1-carboxylic acid methyl ester hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 70083948 | HCID 70083948 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,3-Dihydro-1H-isoindole-1-carboxylic acid methyl ester hydrochloride | HCID 12278923 | — |
| Product | HCID 20405955 | HCID 20405955 | — |
Reaction Steps
Octahydro-1H-isoindole-1-carboxylic acid hydrochloride used as an intermediate in this preparation is obtained by the following method. Following a procedure given in Gazz. Chim. Ital, 106, 65(1976), 2,3-dihydro-1H-isoindole-1-carboxylic acid, methyl ester, hydrochloride is prepared. This compound, 2.14 g, is dissolved in 100 ml of methanol and 5 ml of acetic acid and hydrogenated over 0.5 g of 10% rhodium/carbon catalyst. The catalyst is removed by filtration and the filtrate is concentrated to give a residue which solidifies on trituration with ether. Recrystallization from methanol-ether gives a pure sample of methyl octahydro-1H-isoindole-1-carboxylate hydrochloride, mp 181°-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04503043 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-e4b7cfefe94b495a964fd0b2dab6408f |
| Source note | uspto-grants-1985_03 |