HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 66592542, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 66592500 | HCID 66592500 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66592542 | HCID 66592542 | 96% |
Reaction Steps
A solution of ethyl 2-(7-methoxy-1-benzofuran-3-yl)ethylcarbamate (from step 4) (0.649 g, 2.5 mmol), paraformaldehyde (0.150 g, 5.0 mmol) and 4-toluene sulphonic acid (0.0475 g, 0.125 mmol) was subjected to Dean-Stark for 2-3 hrs. After cooling to RT, water was added and organic layer was separated dried over anhy. sodium sulphate and concentrated. On purification on silica gel, it yielded ethyl 8-methoxy-3,4-dihydro[1]benzofuro[2,3-c]pyridine-2(1H)-carboxylate (96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943634B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-03c3ff2a2197462f85acf7d5ebecd350 |
| Source note | uspto-grants-2011_05 |