HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 10-Benzo[1,3]dioxol-5-yl-5-iodo-9H-furo[3',4':6,7]naphtho[1,2-d][1,3]dioxol-7-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Helioxanthin | HCID 177023 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 10-Benzo[1,3]dioxol-5-yl-5-iodo-9H-furo[3',4':6,7]naphtho[1,2-d][1,3]dioxol-7-one | HCID 5273812 | 55.4% |
Reaction Steps
N-iodosuccinimide (13.6 mg, 0.06 mmol) and concentrated H2SO4 (5 μL) was added to a solution of 2 (14 mg, 0.04 mmol) in acetonitrile (1 mL). The mixture was stirred at room temperature for 36 h, concentrated at reduced pressure, and then diluted with ether (30 mL). The same workup and purification procedure as described for the isolation of 37 afforded 39 (10.5 mg, 55%) as a yellow powder. mp 255° C. (decomp.); 1H NMR (CDCl3) δ 8.78 (s, 1H, H4), 7.93 (s, 1H, H6), 6.75-6.90 (m, 3H, H2′+H5′+H6′), 6.08 (AB, 2H, 3′,4′-OCH2O—, Δδ=8.7 Hz, J=1.5 Hz), 5.97 (AB, 2H, 7,8-OCH2O—, Δδ=7.8 Hz, J=1.5 Hz), 5.23 (q, 2H, lactone-CH2—, J=8.7 Hz); MS (EI) m/z 474 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754718B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-d26e73e0f927439ca8c1128299509996 |
| Source note | uspto-grants-2010_07 |