HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092230Generated: October 30, 2026
4-Hydroxybenzaldehyde → HCID 58097238, compound
https://huagongshe.com/reaction/2092230
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 are 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 are added at RT. The mixture is stirred at 160° C. for 16 h. 4000 ml of water are then added, and the mixture is extracted three times with in each case 500 ml of ethyl acetate. The combined organic phases are washed in each case once with 500 ml water and 500 ml of sat. aqueous sodium chloride solution. After drying over magnesium sulfate, the solvent is removed on a rotary evaporator and the residue is 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 | US08440700B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-56b1055043594a15b4791c7dd93df15e |
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| Source note | uspto-grants-2013_05 |
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