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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651879Generated: November 2, 2026

Ethyl Acetate → HCID 86757339, compound

https://huagongshe.com/reaction/651879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-(Benzyloxy)-N-(tert-butyloxycarbonyl)-1-iodo-N-(4-penten-1-yl)-2-naphthylamineHCID 10697779—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86757339HCID 8675733980%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 81 (44 mg, 81 μmol) in THF (3 mL) was treated sequentially with a solution of NaIO4 (35 mg, 162 μmol, 2 equiv) in 0.5 mL H2O and a solution of OSO4 (7.5 mM in THF, 0.53 mL, 4 μmol, 0.05 equiv). The reaction mixture was stirred for 6 h at 25° C. EtOAc (20 mL) was added and the organic layer was dried (Na2SO4), filtered through Celite, and the solvent removed under vacuum. Chromatography (SiO2, 1×15 cm, 15% EtOAc-hexane) afforded 110 (35 mg, 80%) as an oil: 1H NMR (CDCl3, 400 MHz) δ 9.73 (t, J=1.3 Hz, 1H), 8.32 (d, J=8.2 Hz, 1H), 8.20 (d, J=8.4 Hz, 1H), 7.61-7.49 (m, 4H), 7.42-7.32 (m, 3H), 6.77 and 6.72 (two s, 1H), 5.32-5.25 (m, 2H), 3.86 (ddd, J=14.0, 8.6 Hz, 6.7 Hz, 1H), 3.47 (m, 1H), 2.48 (m, 2H), 1.93-1.75 (m, 2H), 1.29 and 1.23 (two s, 9H); IR (film) νmax 3064, 3032, 2975, 2930, 2722, 1638, 1616, 1590, 1407, 1160 cm31 1; FABHRMS (NBA-CsI) m/z 678.0095 (M+Cs+, C26H28INO4 requires 678.0117).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281354B1
Source datasetuspto-grants-2001_08
ORD IDord-d8fc0739f82a4d2ba60a7964d87707e1
Source noteuspto-grants-2001_08