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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747561Generated: October 31, 2026

Oxygen → HCID 11697437, compound

https://huagongshe.com/reaction/747561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 11698173HCID 11698173—
CatalystTriphenylphosphineHCID 11776—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
ProductHCID 11697437HCID 1169743777.2%

Reaction Conditions

Temperature115 °C

Reaction Steps

217.5 g (478.5 mmol) of hexadecyl (2-bromo-4-methylphenyl)carbamate, 0.5 g (0.7 mmol) of bis(triphenylphosphine)palladium dichloride and 2.5 g (9.3 mmol) of triphenylphosphine were introduced into an autoclave. The autoclave was closed, flushed with nitrogen and an oxygen-free solution of 78.1 g (565.3 mmol) of potassium carbonate in 400 ml of water is added. The autoclave is evacuated and then 2 bar of carbon monoxide are injected and heated to 115° C. The pressure is subsequently adjusted to 8 bar. After CO uptake ceases, the mixture is cooled to RT and 200 ml of toluene are added. The pH is adjusted to 2 with 2M aqueous HCl solution, and the organic phase is separated off. The aqueous phase is extracted anew with 100 ml of toluene, the organic phase is separated off, and the two toluene extracts are combined. Removal of the solvent in vacuo results in 154.9 g (369.2 mmol, 77%) of 2-hexadecyloxycarbonylamino-5-methylbenzoic acid in the form of a pale yellow-coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396952B2
Source datasetuspto-grants-2008_07
ORD IDord-4b3b30f974a14dc58b0689002fa895bb
Source noteuspto-grants-2008_07