HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356746Generated: October 25, 2026
Potassium trimethylsilanolate → N-tert-butoxycarbonylaminomethylsalicylic acid
https://huagongshe.com/reaction/356746
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium trimethylsilanolate | HCID 23668039 | — |
| Reactant | methyl N-tert-butoxycarbonylaminomethyl-salicylate | HCID 54558375 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-tert-butoxycarbonylaminomethylsalicylic acid | HCID 54424118 | 81% |
Reaction Steps
Methyl N-tert-butoxycarbonylaminomethylsalicylate (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-butoxycarbonylaminomethylsalicylic 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 | US05837878 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-06a1f7308262480a9f0bb7cb8ef4a5c7 |
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| Source note | uspto-grants-1998_11 |
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