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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987316Generated: October 29, 2026

4-tert-Butylbenzoyl chloride → HCID 69629012, compound

https://huagongshe.com/reaction/987316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-Butylbenzoyl chlorideHCID 74372—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86595065HCID 86595065—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69629012HCID 6962901289%

Reaction Steps

3-{4-[2-(4-Aminophenyl)ethoxy]phenyl}-(S)-2-ethoxypropanoic acid hydro chloride (described in Example 56a) (0.2 g; 0.547 mmole) was dissolved in tetrahydrofurane (5 ml). Sodium hydrogencarbonate (0.053 g; 0.631 mmole) was added and the mixture was stirred for a little while. 4-tert-Butylbenzoyl chloride (0.118 g; 0.6 mmole) was added. The reaction mixture was stirred overnight and then evaporated to dryness. Dichloromethane and water were added to the residue and the phases were separated. The organic phase was dried with magnesium sulfate and the solvent was evaporated. Chromatography of the residue on silica gel (Isolute, SI) using dichloromethane:heptane (1:1), dichloromethane and finally methanol:dichloromethane (1:99) as eluants gave 0.238 g (89% yield) of 3-{4-[2-{4-(4-[tert-butyl]benzoyl)aminophenyl}ethoxy]phenyl}-2-(S)-ethoxypropanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630600B1
Source datasetuspto-grants-2003_10
ORD IDord-9e0ca8fcd0bf46d091d7354787f756ff
Source noteuspto-grants-2003_10