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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956013Generated: November 1, 2026

Potassium trimethylsilanolate → N-tert-butoxycarbonylaminomethylsalicylic acid

https://huagongshe.com/reaction/1956013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium trimethylsilanolateHCID 23668039—
Reactantmethyl N-tert-butoxycarbonylaminomethyl-salicylateHCID 54558375—
SolventTetrahydrofuranHCID 8028—
ProductN-tert-butoxycarbonylaminomethylsalicylic acidHCID 5442411881%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05777148
Source datasetuspto-grants-1998_07
ORD IDord-f083de0743a641c78f9d2b7039ddb20e
Source noteuspto-grants-1998_07