HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenol → 1-Benzofuran-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | Benzofuran, 5-bromo- | HCID 90015 | — |
| Product | 1-Benzofuran-5-carbaldehyde | HCID 2773875 | — |
Reaction Steps
benzo[b]furan-5-carboxaldehyde was prepared from 5-bromobenzo[b]furan (prepared from 4-bromophenol and bromoacetaldehyde diethyl acetal by the general method described in J. Chem. Soc. Perkin 1, 1972, 556) following essentially the same procedure as that described in (b) above. Benzo[b]furan-5-carboxaldehyde was obtained as an oil. Pmr spectrum (CDCl3 ; δ in ppm): 6.90 (1H, d); 7.55-7.93 (3H, m); 8.15 (1H, d); 10.08 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04664693 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-6afed5888439414b933ffeb56dbfa1b0 |
| Source note | uspto-grants-1987_05 |