Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Levodopa | HCID 6047 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | Hydrochloric Acid | HCID 313 | 99% |
| Product | HCID 11790865 | HCID 11790865 | — |
Reaction Steps
To 30 mL of EtOH at −5° C. was added, with stirring, 0.37 mL of SOCl2 slowly. The clear colorless solution was cooled to −5° C. and 1 g of L-Dopa was added. After 5 min, the resulting solution was refluxed overnight. The solution was concentrated to afford 164 as HCl salt (1.30 g, 99%). 1H NMR (DMSO): δ 1.29 (t, 3H, J=7.4 Hz), 3.03 (m, 1H), 3.15 (m, 1H), 4.21 (m, 1H), 4.27 (m, 2H), 4.35 (sl, 3H), 6.60 (d, 1H, J=7.9 Hz), 6.74 (s, 1H), 6.82 (d, 1H, J=7.9 Hz), 8.63 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08802666B2 |
|---|
| Source dataset | uspto-grants-2014_08 |
|---|
| ORD ID | ord-53f85047c7904038bb1afdf1ac4f3e1e |
|---|
| Source note | uspto-grants-2014_08 |
|---|