HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892856Generated: October 30, 2026
Dimethyl Sulfide → 3-Hydroxy-4-methylbenzaldehyde
https://huagongshe.com/reaction/892856
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | 3-Hydroxy-4-methylbenzoic acid | HCID 68512 | — |
| Reactant | Cornforth reagent | HCID 2724130 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Hydroxy-4-methylbenzaldehyde | HCID 585182 | 33.4% |
Reaction Steps
To a solution of 3-hydroxy-4-methylbenzoic acid (15.22 g, 0.1 mole) in THF (250 mL) was added borane.dimethylsulfide (32.0 mL of a 10.0M solution, 0.32 mole) dropwise. Upon completion of addition, the reaction was stirred for 18 hrs. It was then quenched dropwise by the slow addition of aqueous 10% HCl (250 mL) and extracted with ethylacetate (3×250 mL). The organics were combined, dried with MgSO4 and concentrated. The resulting residue was taken up in CH2Cl2 (500 mL) and pyridinium dichromate (45.15 g, 0.12 mole) was added. The resulting mixture was stirred for 48 hrs. It was then filtered through Celite and concentrated. The resulting residue was chromatographed (silica gel, ether:hexanes, 30:70) to afford 4.55 g of 3-hydroxy-4-methylbenzaldehyde as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05120752 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-d0360e7d92304200b3201efd0499265f |
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| Source note | uspto-grants-1992_06 |
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