HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616910Generated: October 27, 2026
Formaldehyde → 7-Iodo-1,2,3,4-tetrahydro[1]benzofuro[2,3-c]pyridine
https://huagongshe.com/reaction/1616910
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-(6-Iodobenzofuran-3-yl)ethanamine hydrochloride | HCID 67324003 | — |
| Catalyst | Formaldehyde | HCID 712 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 7-Iodo-1,2,3,4-tetrahydro[1]benzofuro[2,3-c]pyridine | HCID 67324876 | 103.8% |
Reaction Steps
Paraformaldehyde (8.9 g, 0.297 mol) was added to a solution of 2-(6-iodo-1-benzofuran-3-yl)ethanamine hydrochloride (80 g; 0.247 mol) in 1N HCl (500 mL) under N2. After 2 h stirring at 70° C., another portion of paraformaldehyde (740 mg) was added. The reaction mixture was cooled down to r.t., filtered, the resulting solid was washed with 1N HCl (100 mL), dried overnight under house vacuum to afford 76.7 g of the title product as a hydrochloric acid salt. 1H-NMR (400 MHz, CDCl3): δ 2.06 (bt, 2H), 2.92 (bt, 2H), 4.37 (s, 2H), 7.45 (d, 1H) 7.62 (dd, 1H), 8.05 (d, 1H), 10.04 (bs, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08765779B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-aa96e2549f954b9093dec4d12cfdf7d5 |
|---|
| Source note | uspto-grants-2014_07 |
|---|