HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546821Generated: October 28, 2026
Tetrabutylammonium Fluoride → HCID 57709019, compound
https://huagongshe.com/reaction/546821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | HCID 57708913 | HCID 57708913 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57709019 | HCID 57709019 | 93.3% |
Reaction Steps
Tetra-n-butylammonium fluoride (1 M solution in tetrahydrofuran, 0.2 mL, 0.2 mmol) and tetrahydrofuran (1 mL) were added to 3-[4′-(1-{4-[3-(t-butyl-dimethyl-silanyloxy)-4,4-dimethyl-pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2′-methyl-biphenyl-3-yl]-propionic acid methyl ester (Example 12-(2); 0.016 g, 0.025 mmol), and the mixture was stirred at 60° C. for four hours. A 30% sodium dihydrogenphosphate aqueous solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by preparative TLC (hexane/ethyl acetate=1/1) to give the title compound (0.012 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935688B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-e752a7b9470f49cf8ed272293bf82e2b |
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| Source note | uspto-grants-2011_05 |
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