HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Benzoyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride | HCID 2724135 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Benzoyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid | HCID 570005 | — |
Reaction Steps
This compound was prepared according to Hein et. al., J. Amer. Chem. Soc.; 1962, 84, 4487-4494, incorporated by reference herein in its entirety. Thus, a slurry of 1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid hydrochloride (20.3 g, 95 mmol) in 2N NaOH (150 ml) was treated with benzoyl chloride (13.4 ml, 114 mmol) dropwise over 30 minutes. The mixture was stirred a further 1.5 hours, acidified to pH 2-3 (4N HCl), and extracted with ethyl acetate. The organic phase was washed with water and brine, dried over anhydrous magnesium sulfate, filtered and concentrated to afford 16.4 g (61) of the title compound following recrystallization (acetone/water); MS: 280 m/z (M-H)-.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05952328 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-b8b70703deac4ded93d5efb4e749d480 |
| Source note | uspto-grants-1999_09 |