HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 6-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 6-Fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid | HCID 57947941 | — |
| Product | Methyl 6-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylate | HCID 57947410 | — |
Reaction Steps
To a suspension of 6-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid in methanol (500 mL) was added SOCl2 (50 mL). The reaction mixture was then refluxed for 1 h until LC-MS indicated the completion of the reaction. The mixture was concentrated, and the resulting residue was dissolved in a mixture of EtOAc (1 L) and sat. sodium bicarbonate solution (500 mL). The organic layer was separated, washed with water and brine, dried over Na2SO4, and concentrated under reduced pressure to give 6-fluoro-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester as an oil (92 g). LRMS (M+H+) m/z 210.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759374B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-472e69e60d9545f7b1af2a7a845815b2 |
| Source note | uspto-grants-2014_06 |