HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalic acid dihydrate → N-Benzyl-N-methyl-2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanamine oxalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalic acid dihydrate | HCID 61373 | — |
| Reactant | N-benzyl-N-methyl-2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanamine | HCID 17751624 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-Benzyl-N-methyl-2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanamine oxalate | HCID 17751623 | — |
Reaction Steps
N-Benzyl-N-methyl-2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanamine oxalate is prepared from a solution of N-benzyl-N-methyl-2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanamine in acetone with a slightly excess of HO2CCO2H.2H2O. Slightly pinkish solid. M.p.=123-125° C. 1H NMR (300 MHz, CD3OD): δ 1.37 (m, 1H), 1.65-2.13 (m, 5H), 2.49 (m, 2H), 2.70 (m, 1H), 2.78 (s, 3H), 3.23 (m, 2H), 3.43 (s, 3H), 4.32 (m, 2H), 5.80 (d, J=2.8 Hz, 1H), 6.46 (d, J=2.8 Hz, 1H), 7.48 (s, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481567B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-97851242f3ee4d8a95a0de7f8adeb530 |
| Source note | uspto-grants-2013_07 |