HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403013Generated: October 30, 2026
4-Hydroxybenzaldehyde → HCID 58097238, compound
https://huagongshe.com/reaction/403013
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
An amount of 31.2 g (255.4 mmol) of 4-hydroxybenzaldehyde was introduced in 400 ml of dry DMF and admixed at RT with 105.7 g (766.1 mmol) of potassium carbonate and also 50.0 g (332.0 mmol) of (S)-(−)-3-chloro-1,2-propanediol acetonide. The batch was stirred at 160° C. for 16 hours. The batch was then admixed with 4000 ml of water and extracted with three times 500 ml of ethyl acetate. The combined organic phases were washed once each 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 (eluent gradient: ethyl acetate/petroleum ether 1:9→2:8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741834B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-1108c9725b7c43dab7c405ed6eed5949 |
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| Source note | uspto-grants-2014_06 |
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