Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836747Generated: October 29, 2026

Methanol → alpha-Methylhydrocinnamic acid

https://huagongshe.com/reaction/1836747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-(2-Methylphenyl)prop-2-enoic acidHCID 98306—
ReactantHCID 178418361HCID 178418361—
Productalpha-Methylhydrocinnamic acidHCID 99862—

Reaction Steps

4.73 mg (0.0126 mmol) of [Rh(NBD)2]BF4 and 12.2 mg (0.0131 mmol) of B1c are placed in a flask provided with a magnetic stirrer and blanketed with argon by repeatedly evacuating the flask and flushing it with argon. 5 ml of degassed methanol are then added and the mixture is stirred for 15 minutes. 0.405 g (2.497 mmol) of 2-methylcinnamic acid and 5 ml of degassed methanol are subsequently introduced into a 10 ml Schlenk flask filled with an argon atmosphere. Stirring is continued until a homogeneous solution is formed. The solution is injected by means of a steel capillary into a 50 ml steel autoclave filled with argon. Finally, 5 bar of hydrogen are introduced in three flushing cycles (argon 20 bar/hydrogen 20 bar). The hydrogenation is started by switching on the stirrer and is carried out at 25° C. The course of the reaction is followed via the hydrogen consumption (pressure decrease in the hydrogen reservoir). After a reaction time of 20 hours, the conversion is found to be complete. The enantiomeric purity of 2-methyl-3-phenylpropionic acid is 81.7% of (R).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777567B2
Source datasetuspto-grants-2004_08
ORD IDord-77d9ed8aa24147bf8c21f3749b913d87
Source noteuspto-grants-2004_08