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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254170Generated: November 1, 2026

TBAF tetrahydrofuran → HCID 57814800, compound

https://huagongshe.com/reaction/1254170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTBAF tetrahydrofuranHCID 11078149—
ReactantHCID 57814810HCID 57814810—
ProductHCID 57814800HCID 5781480079.3%

Reaction Steps

A solution of silyl ether 7 (270 mg, 0.43 mmol) was stirred at 30° C. with 2 mL (2 mmol) of 1.0M TBAF/THF in a vial for 20 h. TLC indicated starting material was mostly desilylated and the reaction was concentrated in vacuo. The residual crude products were taken up in 50 mL of ethyl acetate and washed sequentially with saturated ammonium chloride (50 mL), brine (50 mL), and dried over 10 g of anhydrous sodium sulfate. The mixture was filtered and concentrated in vacuo. The residual products were purified by flash column chromatography on 20 g of silica gel eluted in 1:1 hexanes:EtOAc, then straight EtOAc. Combination of appropriate fractions and removal of the solvents yielded 175 mg (79%) of pure diol 8 as an oil; 1H NMR (CDCl3): 1.18 (d, J=6 Hz, 3H), 1.38-1.84 (m, 13H), 1.91 (m, 1H), 2.00-2.40 (m, 11H), 3.47 (m, 1H), 3.81 (m, 2H), 3.99 (m, 1H), 4.09 (m, 2H), 4.54-4.72 (m, 3H), 5.21-5.66 (m, 6H), 5.92 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455547B2
Source datasetuspto-grants-2013_06
ORD IDord-8485370d33c84de79c8d81fc0515adbe
Source noteuspto-grants-2013_06