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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919899Generated: November 1, 2026

Hydrochloric Acid → 4-{3-Tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoic acid

https://huagongshe.com/reaction/1919899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 4-{3-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoateHCID 57611911—
ReactantHCID 178504318HCID 178504318—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-{3-Tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoic acidHCID 57611917—

Reaction Steps

Methyl 4-{3-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoate (0.40 g, 1.05 mmol) was dissolved in THF (10 mL). KOSiMe3 (0.27 g, 2.10 mmol) was added to the solution and allowed to stir overnight at room temperature under nitrogen. Saturated ammonium chloride was added and allowed to stir. Hydrochloric acid (2 mL, 1M solution) was added. The reaction was diluted with ethyl acetate and separated. The aqueous layer was extracted three times with ethyl acetate. The combined organic layer was dried with sodium sulfate, filtered, and concentrated. The resulting material was purified by HPLC. MS: cal'd 365 (MH+), exp 388 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168658B2
Source datasetuspto-grants-2012_05
ORD IDord-e37f55ae093d4de7840b0ffd3b575365
Source noteuspto-grants-2012_05