HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254170Generated: November 1, 2026
TBAF tetrahydrofuran → HCID 57814800, compound
https://huagongshe.com/reaction/1254170
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | TBAF tetrahydrofuran | HCID 11078149 | — |
| Reactant | HCID 57814810 | HCID 57814810 | — |
| Product | HCID 57814800 | HCID 57814800 | 79.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455547B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-8485370d33c84de79c8d81fc0515adbe |
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| Source note | uspto-grants-2013_06 |
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