HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589537Generated: October 25, 2026
Diethyl phenylmalonate → 2-Phenyl-1,3-propanediol
https://huagongshe.com/reaction/589537
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl phenylmalonate | HCID 66514 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Phenyl-1,3-propanediol | HCID 254178 | 63% |
Reaction Steps
Sodium dihydrogen phosphate (58.3 g) was added to a solution of 50 g of diethyl phenylmalonate in 350 ml of ethanol. The mixture was cooled to 5-7° C. and a solution of 16.7 g of sodium borohydride in 38 ml of 0.2% NaOH was gradually added. The mixture was stirred for additional 2 hours and the Ethanol was distilled out. The reaction was quenched by adding 132 ml of water followed by heating to 50° C.-60° C. for 2 hours. The solution was then basified with 50% NaOH and extracted with ethyl acetate. The organic layer was washed with water and evaporated to dryness. The precipitate was crystallized from toluene. 20 g of 2-phenyl-1,3-propanediol was obtained with a yield of 63%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233898B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-b88aeaad75c048ccbe383ea0a0fd611f |
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| Source note | uspto-grants-2016_01 |
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