HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851180Generated: November 1, 2026
Phenylacetaldehyde → HCID 67027749, compound
https://huagongshe.com/reaction/1851180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetaldehyde | HCID 998 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Bromo-4-(dimethoxymethyl)benzene | HCID 688342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67027749 | HCID 67027749 | — |
Reaction Steps
A mixture of Mg turnings 2.4 g (0.1 mol) and 2 mL 1-bromo-4-(dimethoxymethyl)benzene (0.012 mol) in THF (100 mL) was heated under nitrogen atmosphere until the reaction starts. Subsequently additional 1-bromo-4-(dimethoxymethyl)benzene 14.71 mL (0.088 mol) dissolved in 30 mL THF was added slowly and the reaction refluxed for 1 h mixture to complete formation of the Gringnard reagent. A solution of 11.70 mL phenylacetaldehyde (0.1 mol) in 100 mL THF was added at to 0° C. and the reaction refluxed for 2 h upon completion of the addition. The mixture was worked up by pouring into saturated aqueous NH4Cl and extraction with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and the solvents were evaporated under reduced pressure. The brown-black oily product was used for the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957064B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-eaae717bac734cc9b42a1ce7b7b3bb0e |
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| Source note | uspto-grants-2015_02 |
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