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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577609Generated: October 28, 2026

(6-Iodo-2H-1,3-benzodioxol-5-yl)methanol → 6-iodobenzo[d][1,3]dioxole-5-carbaldehyde

https://huagongshe.com/reaction/577609

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Iodo-2H-1,3-benzodioxol-5-yl)methanolHCID 323453—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product6-iodobenzo[d][1,3]dioxole-5-carbaldehydeHCID 1085003277%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040556B2
Source datasetuspto-grants-2015_05
ORD IDord-5d9633089404484896e3087f5e95d12f
Source noteuspto-grants-2015_05