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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450040Generated: November 2, 2026

2,2,6,6-Tetramethylbenzo[1,2-d:4,5-d']bis([1,3]dioxole) → Tris(2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']bis(1,3)dioxole-4-yl)methanol

https://huagongshe.com/reaction/1450040

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,6,6-Tetramethylbenzo[1,2-d:4,5-d']bis([1,3]dioxole)HCID 10922085—
ReactantBis(2,2,6,6-tetramethylbenzo-(1,2-d:4,5-d']bis(1,3)dioxole-4-yl)ketoneHCID 18943092—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductTris(2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']bis(1,3)dioxole-4-yl)methanolHCID 10952571—

Reaction Steps

2,2,6,6-Tetramethylbenzo[1,2-d:4,5-d']bis(1,3)dioxole (8.80 g, 40.00 mmol, Example 5) was dissolved in THF (100 mL) and cooled to -20° C. n-Butyllithium (25.0 mL, 40.0 mmol, 1.6M) was added and the temperature was adjusted to ambient temperature over a period of 30 minutes and then recooled to -20° C. Bis(2,2,6,6-tetramethylbenzo-[1,2-d:4,5-d']bis(1,3)dioxole-4-yl)ketone (18.80 g, 39.83 mmol, Example 57) was added and the temperature was once more adjusted to room temperature and the mixture was stirred for 18 hours. The mixture was then poured on water/AcOH (100 mL, 2% AcOH) and extracted with diethyl ether (2×100 mL). The organic phase was washed with water (2×100 ml) and dried (Na2SO4). The solvent was evaporated and the product was washed with petroleum ether (20 mL, 40°-60° C.). Yield 10.80 g (64.1%). Spectral data see example 44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599522
Source datasetuspto-grants-1997_02
ORD IDord-3b59da73ed354d938dfa020edd1ffbe0
Source noteuspto-grants-1997_02