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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590694Generated: October 31, 2026

Chloroform → Methyl 2-[3-(phenylhydroxymethyl)phenyl]propionate

https://huagongshe.com/reaction/1590694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantMethyl 2-(3-benzoylphenyl)propanoateHCID 529083—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductMethyl 2-[3-(phenylhydroxymethyl)phenyl]propionateHCID 1049226897%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 164 g of methyl 2-(3-benzoylphenyl)propionate in 1100 mL methanol at a 0° C., 14 of sodium borohydride were added, keeping the temperature between 7 and 10° C. After 2 hours of stirring at 0° C., TLC (silica-gel/chloroform) showed total consumption of starting material. The solvent was evaporated under vacuum. The residue was dissolved in 400 mL of methylene chloride. The solution was washed three times with 250 ml of 1% hydrochloric acid, until acid pH, and then with saturated sodium chloride solution, until neutral pH. After evaporation of the solvent, the oily colourless residue wheighted 160,0 g (97% yield) and was identified as the title compound. IR Spectrum (film), cm-1 : 3480 (broad), 3080-2880, 1730, 1455, 1200, 1175, 1110, 700. In the 200 MHz 1H-NMR apparatus the signal of CH3 appears as two doublets of similar intensity, indicating the presence of the two possible diasteromers. By following analogous procedures, compounds IVc of Table 2 were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05204365
Source datasetuspto-grants-1993_04
ORD IDord-45a2997a8783484aa59083cec5702b38
Source noteuspto-grants-1993_04