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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378175Generated: November 1, 2026

Piperonal → Bis(1,3-benzodioxol-5-yl)methanol

https://huagongshe.com/reaction/2378175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperonalHCID 8438—
Reactant1-Bromo-3,4-(methylenedioxy)benzeneHCID 75831—
Reactant(2,3-Dihydrobenzo[1,4]dioxin-6-yl)-(3,5-dimethoxyphenyl)methanolHCID 69202534—
ReactantButyllithiumHCID 178418339—
ProductBis(1,3-benzodioxol-5-yl)methanolHCID 38422583%

Reaction Steps

Benzo[1,3]dioxole-5-carbaldehyde (1.80 g, 11.96 mmol), 5-bromobenzo[1,3]dioxole (2.65 g, 13.16 mmol), and n-butyl lithium (5.26 ml, 13.16 mmol) were treated in the same manner as described above for the synthesis of (2,3-dihydrobenzo[1,4]dioxin-6-yl)-(3,5-dimethoxyphenyl)methanol. The crude material was purified via flash column chromatography (5% EtOAc in hexane gradient to 40% EtOAc in hexane in about 40 min.) to give bis-benzo[1,3]dioxol-5-yl-methanol as a light brown oil (2.69 g, 83%): 1HNMR (CDCl3) 6.86-6.74 (m, 6H, Ar), 5.93 (s, 4H, 2CH2), 5.68 (d, J=3 Hz, 1H, CHOH), 2.16 (d, J=3 Hz, 1H, OH). The product was carried over to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470723B2
Source datasetuspto-grants-2008_12
ORD IDord-8f26af6044ec424b865d6be56a481163
Source noteuspto-grants-2008_12