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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400286Generated: October 30, 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/400286

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 numberUS05827501
Source datasetuspto-grants-1998_10
ORD IDord-b8069e9e778f4e47a0b569f55aebeba3
Source noteuspto-grants-1998_10