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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549084Generated: October 30, 2026

Iodine → HCID 67157927, compound

https://huagongshe.com/reaction/549084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium HydroxideHCID 14797—
ReactantIndole, 6-(benzyloxy)-5-methoxy-HCID 17051—
ReactantSodium SulfiteHCID 24437—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 67157927HCID 67157927—

Reaction Steps

A solution of 6-benzyloxy-5-methoxyindole (1.90 g, prepared according to procedure described by Benigni, J. D. and Minnis, R. L., J. Heterocycl. Chem. 1965, 2, 387 and Sinhababu, A. K. and Borchardt, R. T., J. Org. Chem. 1983, 48, 3347) in dry dimethylformamide (37.5 mL) was treated with ground potassium hydroxide (1.24 g) and a solution of iodine (1.96 g) in dry dimethylformamide (37.5 mL) dropwise at room temperature. The reaction mixture was stirred at room temperature for 2 hours, then treated with 4-dimethylaminopyridine (69 mg) followed by a solution of di-tert-butyldicarbonate (2.05 g) in dry dimethylformamide and stirring was continued for a further 1 hour. The reaction mixture was poured into aqueous sodium sulfite solution (0.2%). The aqueous phase was extracted three times with ethyl acetate (100 mL). The combined organic phases were washed with water (100 mL), then with brine (100 mL), then dried over magnesium sulfate and then evaporated. The residue was subjected to flash column chromatography on silica eluting with a mixture of cyclohexane and ethyl acetate (1:9, v/v) to give the title compound (3.35 g) as a white solid. TLC: RF=0.58 (dichloromethane). MS: EI (70 eV); m/z=479 M+. (45%); 423 (100%); 332 (75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943616B2
Source datasetuspto-grants-2011_05
ORD IDord-5311cfaa22cf43819e76d79e4cd36aac
Source noteuspto-grants-2011_05