HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039149Generated: October 26, 2026
Tetrabutylammonium Fluoride → 7-[4-(4-Methoxyphenyl)thiazol-2-yl]heptan-1-ol
https://huagongshe.com/reaction/1039149
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 2-[7-(Tert-butyldimethylsilanyloxy)heptyl]-4-(4-methoxyphenyl)thiazole | HCID 68489930 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 7-[4-(4-Methoxyphenyl)thiazol-2-yl]heptan-1-ol | HCID 68491411 | 89.4% |
Reaction Steps
Add a solution of 1 N tetra-n-butylammonium fluoride (25.0 mmol, 25 mL, 1 M solution in THF) dropwise over 10 minutes to a solution of 2-[7-(tert-butyldimethylsilanyloxy)heptyl]-4-(4-methoxyphenyl)thiazole (6.27 g, 14.9 mmol) in anhydrous THF (50 mL) at 0° C. under nitrogen and stir the mixture for 30 minutes at 0° C. and then stir at room temperature for 3 hours. Dilute the mixture with brine (150 mL) and extract with ethyl acetate (100 mL×3). Dry the combined organic extracts over magnesium sulfate and remove the solvent under reduced pressure. Purify the crude product by flash column chromatography on silica gel, eluting with ethyl acetate/hexanes (1:2), to give 7-[4-(4-methoxyphenyl)thiazol-2-yl]heptan-1-ol (4.07 g, 89%): APCI mass spectrum m/z 306 [C17H23NO2S+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552039B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-b4f2fb1e1ed5484ea13286eb909cf934 |
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| Source note | uspto-grants-2013_10 |
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