HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190940Generated: October 30, 2026
Hydrochloric Acid → 6-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochloride
https://huagongshe.com/reaction/1190940
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 6-Methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine | HCID 13853358 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochloride | HCID 57458020 | 63% |
Reaction Steps
Dissolve crude 6-methoxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine (35.1 g, 0.198 mol) in 2B-3 ethanol (250 mL), heat the solution to reflux and add 2M HCl in ethanol (108.9 mL, 0.218 mol, 1.1 equiv.). Slowly add heptane (700 mL) over 10 min, then remove the heating mantle and cool the solution to ambient temperature, and finally continue the cooling with an ice/water mixture. Collect the resulting solid by vacuum filtration and wash with cold ethanol:heptane (1:2) (3×100 mL), air-dry for 15 min under vacuum, then further dry the product in a vacuum oven at 60° C. for 1 h to give the desired intermediate as a white granular solid (35.53 g, 63%): mp 246.6-246.9° C.; 1H NMR (300 MHz, DMSO-d6), δ 9.82 (broad s, 1H), 7.12 (dd, 1H, J=7.6, 7.9), 6.88 (d, 1H J=8.2), 6.78 (d, 1H, J=7.3), 3.75 (s, 3H), 3.20-3.00 (m, 8H); 13C NMR (300 MHz, DMSO-d6), δ 156.2, 141.3, 127.4, 127.2, 121.6, 109.7, 55.7, 44.9, 44.7, 31.6, 21.7; MS (ES+) m/z 178 (M+H)+; Anal. Calc'd for C11H15ClNO: C, 62.12; H, 7.11; N, 6.59. Found: C, 61.95, H, 7.64; N, 6.58.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08680091B2 |
|---|
| Source dataset | uspto-grants-2014_03 |
|---|
| ORD ID | ord-e284ef41a8cc40ffaee8274b3c70333f |
|---|
| Source note | uspto-grants-2014_03 |
|---|