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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382245Generated: October 31, 2026

Sodium Hydroxide → 2-{2-[(9-Butoxy-5',5'-dimethyl-6,7-dihydrospiro-[dibenzo[a,e]cyclopropa[c][8]annulene-1,2'-[1,3]dioxan]-4-yl)oxy]ethoxy}ethanol

https://huagongshe.com/reaction/2382245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-{2-[(9-Butoxy-5',5'-dimethyl-6,7-dihydrospiro-[dibenzo[a,e]cyclopropa[c][8] annulene-1,2'-[1,3]dioxan]-4-yl)oxy]ethoxy}ethyl acetateHCID 66779132—
SolventMethanolHCID 887—
Product2-{2-[(9-Butoxy-5',5'-dimethyl-6,7-dihydrospiro-[dibenzo[a,e]cyclopropa[c][8]annulene-1,2'-[1,3]dioxan]-4-yl)oxy]ethoxy}ethanolHCID 6677893681%

Reaction Steps

A solution of NaOH (1.2 mL, 1.2 mmol, 1 M aqueous solution) was added to solution of acetate 10 (0.593 g, 1.11 mmol) in MeOH:THF (10:3 mL) at room temperature, and the reaction mixture was stirred for 30 minutes at room temperature. The reaction mixture was partially concentrated under reduced pressure, diluted with EtOAc (approximately 25 mL) and water (approximately 10 mL), the organic layer was separated, washed with brine, and dried over anhydrous MgSO4. Solvents were evaporated under reduced pressure, and the residue was separated by chromatography (Hex:ExOAc:CH2Cl2 3:2:1+1.5% of Et3N) to provide 0.493 g (0.89 mmol, 81%) of an alcohol 11 as slightly yellow oil that crystallizes on standing. 1H NMR: 7.65 (dd, J=8.4, 2.4 Hz, 2H), 6.92-6.82 (m, 4H), 4.18 (t, J=4.4 Hz, 2H), 4.04 (t, J=6.4 Hz, 2H), 3.92 (m, 4H), 3.88 (t, J=4.4 Hz, 2H), 3.77 (t, J=4.4 Hz, 2H), 3.68 (t, J=4.4 Hz, 2H), 3.24 (d, J=10.8 Hz, 2H), 2.41 (d, J=10.8 Hz, 2H), 1.76 (p, J=7.2 Hz, 2H), 1.50 (six, J=7.6 Hz, 2H), 1.21 (s, 3H), 1.19 (s, 3H), 0.99 (t, J=7.2 Hz, 3H); 13C NMR: 159.8, 159.2, 147.4, 131.84, 131.75, 131.67, 131.57, 124.4, 123.6, 119.8, 119.1, 116.3, 116.2, 112.2, 84.1, 79.4, 72.8, 69.8, 68.0, 76.7, 62.0, 37.1, 31.5, 30.8, 22.9, 19.4, 14.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258347B2
Source datasetuspto-grants-2012_09
ORD IDord-b497d664129a4065800d7eca9be80a6d
Source noteuspto-grants-2012_09