HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985177Generated: October 29, 2026
Potassium trimethylsilanolate → HCID 54082100, compound
https://huagongshe.com/reaction/985177
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium trimethylsilanolate | HCID 23668039 | — |
| Reactant | HCID 69733477 | HCID 69733477 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54082100 | HCID 54082100 | 81% |
Reaction Steps
Methyl N-tert-butoxycarbonylaminomethyl-2-hydroxybenzoate (8.7 g, 30.9 mmoles) was dissolved in dry tetrahydrofuran (100 mL), and potassium trimethylsilanolate (4.4 g, 30.9 mmoles, 90% pure) was added. The yellow solution was refluxed for 24 hours, during which time a tan precipitate formed and the solvent turned light brown. The mixture was evaporated to dryness, and the solid was dissolved in cold water (100 mL). The brown solution was chilled in an ice bath, and saturated aqueous potassium hydrogen sulfate solution was used to titrate the stirred solution to pH 2-3. An off-white solid precipitated during the titration. The solid was filtered, washed with cold water, and dried in vacuo over potassium hydroxide to afford 6.7 g, (81% yield) of crude N-tert-butoxycarbonylaminomethyl-2-hydroxybenzoic acid (m.p. 141-144° C., decomposes with effervescence on melting, open capillary, uncorrected).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06870065B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-8b82474b3e064fbfb6a63b8040625137 |
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| Source note | uspto-grants-2005_03 |
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