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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384503Generated: October 27, 2026

Toluene → 5-Amino-2-chlorobenzoic acid 1-allyloxycarbonyl-1-methyl-ethyl ester

https://huagongshe.com/reaction/1384503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosphinic AcidHCID 4124402—
Reactant1-(Allyloxy)-2-methyl-1-oxopropan-2-yl 2-chloro-5-nitrobenzoateHCID 11782392—
CatalystVanadiumHCID 23990—
CatalystHCID 178503042HCID 178503042—
SolventWaterHCID 962—
Product5-Amino-2-chlorobenzoic acid 1-allyloxycarbonyl-1-methyl-ethyl esterHCID 1096850994.8%

Reaction Steps

0.9 g of vanadium-containing active carbon prepared according to Example A1 is added to a solution of 16.1 g of 2-(2-chloro-5-nitrobenzoyloxy)-2-methyl-propionic acid allyl ester and 100 mg of toluene in an autoclave having a stirrer. 82 mg of platinum-carbon catalyst together with 50 mg of hypophosphorous acid and 2 ml of deionised water are placed in a seperate glass vessel, and the mixture is stirred for 10 minutes. The catalyst suspension is then transferred to the autoclave, rinsing the glass vessel with 4 ml of deionised water, and hydrogenated for 2 hours at a temperature of 100° C. and a hydrogen pressure of 20 bar. After cooling and rendering the autoclave inert using nitrogen, the catalyst is filtered off and washed with 20 ml of toluene. After working up by distillation, 14 g of 2-(2-chloro-5-amino-benzoyloxy)-2-methyl-propionic acid allyl ester having a content of 98.9% according to HPLC are obtained (yield 94.8% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258982B1
Source datasetuspto-grants-2001_07
ORD IDord-a620dc1bde02438cb54e14cc86429f31
Source noteuspto-grants-2001_07