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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988093Generated: October 31, 2026

Acetic Acid → HCID 58742366, compound

https://huagongshe.com/reaction/1988093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 68832690HCID 68832690—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58742366HCID 58742366—

Reaction Steps

To a solution of (2R,3S,4aR,10aR)-7-(tert-butyl-dimethylsilanyloxy)-4a-ethyl-2-(pyridin-3-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-2,3-diol (13 mg, 0.03 mmol) and acetic acid (0.05 mL, 0.87 mmol) in tetrahydrofuran (2 mL) was added a 1.0 M solution of tetrabutylammonium fluoride in tetrahydrofuran (0.13 mL, 0.13 mmol). The mixture was stirred overnight at room temperature and the concentrated under vacuum. The residue was taken up in ethyl acetate and filtered through a plug of silica gel. The title compound, a solid (4.2 mg, 43%) was obtained by evaporation of the solvent. 1H NMR (CDCl3) selected signals: δ 9.00 (br s, 1H), 8.50 (d, J=8.3 Hz, 1H), 8.26 (d, J=5.7 Hz, 1H), 7.32 (dd, J=5.7, 7.8 Hz, 1H), 6.94 (d, J=8.3 Hz, 1H), 6.65 (dd, J=2.6, 8.3 Hz, 1H), 6.60 (d, J=2.6 Hz, 1H), 4.23 (dd, J=4.7, 13.0 Hz, 1H). MS: m/e 340 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553877B2
Source datasetuspto-grants-2009_06
ORD IDord-f8263c2198e44c3bb25a408fa66a0a53
Source noteuspto-grants-2009_06