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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Methyl 2-(3-benzoylphenyl)propanoate | HCID 529083 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-[3-(phenylhydroxymethyl)phenyl]propionate | HCID 10492268 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05204365 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-45a2997a8783484aa59083cec5702b38 |
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| Source note | uspto-grants-1993_04 |
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