HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172539Generated: October 29, 2026
Tetrabutylammonium Fluoride → HCID 67246085, compound
https://huagongshe.com/reaction/1172539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 67246220 | HCID 67246220 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67246085 | HCID 67246085 | — |
Reaction Steps
A solution of tetra-n-butylammonium fluoride (6.12 g, 19 mmol) in tetrahydrofuran (20 mL) was added dropwise to a solution of 4-bromo-3-[2-(tert-butyl-dimethyl-silanyloxy)-3-chloro-benzylsulfanyl]-5-methyl-benzoic acid methyl ester (5 g, 96.9 mmol) in tetrahydrofuran (50 mL) under nitrogen at 5° C. and stirring was continued for 0.5 h. It was concentrated, treated with chilled water and extracted with ethyl acetate. The organic layer was washed with water, brine, dried, concentrated and purified using flash chromatography (silica gel, ethyl acetate/pet ether) to obtain the title compound as a white solid. Yield: 3.0 g, (95%); 1H NMR (CDCl3): δ 2.42 (s, 3H, CH3), 3.88 (s, 3H, OCH3), 4.34 (s, 2H, CH2), 6.81 (t, 1H, Ar), 7.29 (t, 2H, Ar), 7.7 (s, 2H, Ar); MS: m/e (EI+) 401 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834001B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-b9e86763d3e847dfba9f49360cd3af10 |
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| Source note | uspto-grants-2010_11 |
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