HuagongsheHuagongshe Chemistry Print Report · For research reference only
(6-Iodo-2H-1,3-benzodioxol-5-yl)methanol → 6-iodobenzo[d][1,3]dioxole-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (6-Iodo-2H-1,3-benzodioxol-5-yl)methanol | HCID 323453 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-iodobenzo[d][1,3]dioxole-5-carbaldehyde | HCID 10850032 | 77% |
Reaction Steps
(6-Iodobenzo[d][1,3]dioxol-5-yl)methanol (2.7 g, 9.7 mmol) in dry CH2Cl2 was added dropwise to PCC (3.1 g, 14.6 mmol) in dry CH2Cl2 at 0° C. under N2 atmosphere. The mixture was stirred at room temperature for 20 h. After reaction, the crude product was purified by column chromatography on silica gel (petroleum ether) to obtain 6-iodobenzo[d][1,3]dioxole-5-carbaldehyde (2 g, 77%) as white solid. LCMS: 277[M+1]+; 1H NMR (DMSO-d6) δ 6.20 (s, 2H), 7.28 (s, 1H), 7.61 (s, 1H), 9.79 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040556B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-5d9633089404484896e3087f5e95d12f |
| Source note | uspto-grants-2015_05 |