HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479208Generated: October 27, 2026
Phosphorus oxychloride → 2-Methyl 4-benzyloxybenzaldehyde
https://huagongshe.com/reaction/479208
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | m-(Benzyloxy)toluene | HCID 70035 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Boron | HCID 5462311 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Methyl 4-benzyloxybenzaldehyde | HCID 2759806 | 17% |
Reaction Steps
Dry N,N-dimethylformamide (34.2 ml, 444 mmol) was added dropwise with stirring and cooling under an argon atmosphere to phosphorous oxychloride (18.3 ml, 200 mmol) at such a rate that the temperature did not exceed 10° C. After 30 min stirring at 0° C., a solution of 1-benzyloxy-3-methyl-benzene (22 g, 111 mmol) in N,N-dimethylformamide (22 ml) was added dropwise within 30 min (for the preparation of 1-benzyloxy-3-methyl-benzene see: D. Bogdal, J. Pielichowski, A. Boron, Syn. Commun. 1998, 28, 3029-3039). The reaction mixture was stirred 30 min at ambient temperature and then continuously heated to 110° C. After 10 min at 110° C., the mixture was kept at 90° C. for 3.5 h, cooled to 10° C., neutralized with 25% aqueous sodium acetate, with cooling, and extracted with ethyl acetate. The combined organic layers were washed with saturated aqueous sodium bicarbonate and brine and dried over sodium sulfate. Removal of the solvent under reduced pressure gave a brown oil which was purified by column chromatography (silica gel, hexane/AcOEt=19/1) to give 4.3 g (19 mmol, 17%) of the title compound as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06642389B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-aeed95b6b17745eca10ca011fe9dd656 |
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| Source note | uspto-grants-2003_11 |
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