HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913492Generated: November 2, 2026
4-Hydroxybenzaldehyde → HCID 58097238, compound
https://huagongshe.com/reaction/1913492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178521079 | HCID 178521079 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58097238 | HCID 58097238 | — |
Reaction Steps
31.2 g (255.4 mmol) of 4-hydroxybenzaldehyde were initially charged in 400 ml of dry DMF, and 105.7 g (766.1 mmol) of potassium carbonate and 50.0 g (332.0 mmol) of (S)-(−)-3-chloro-1,2-propanediol acetonide were added at RT. The mixture was stirred at 160° C. for 16 h. 4000 ml of water were then added, and the mixture was extracted three times with in each case 500 ml of ethyl acetate. The combined organic phases were washed in each case once with 500 ml of water and 500 ml of saturated aqueous sodium chloride solution. After drying over magnesium sulfate, the solvent was removed on a rotary evaporator and the residue was purified by column chromatography on silica gel 60 (mobile phase gradient: ethyl acetate/petroleum ether 1:9→2:8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609686B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-024d762e3b39433abee8b46557289a93 |
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| Source note | uspto-grants-2013_12 |
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