HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784662Generated: November 3, 2026
Methyl iodide → 4-(1,2,5,6-Tetrahydro-1-methyl-3-pyridinyl)benzenemethanol
https://huagongshe.com/reaction/1784662
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 4-(Pyridin-3-yl)benzaldehyde | HCID 3693046 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(1,2,5,6-Tetrahydro-1-methyl-3-pyridinyl)benzenemethanol | HCID 67117383 | 72.1% |
Reaction Steps
Methyl iodide (0.8 ml, 12.9 mmol) was added to a solution of 4-(3-pyridyl)benzaldehyde (0.78 g, 4.3 mmol) in dichloromethane and stirred 2 days. Additional methyl iodide (0.8 ml, 12.9 mmol) was added and stirred for 3 hr. After removal of the solvent, methanol was added to the residue and ice-cooled. Sodium tetrahydroborate (6.4 g, 17.0 mmol) was added to the solution and stirred for 1.5 hr with warming to room temperature. Organic solvents were removed under reduced pressure after addition of water and extracted with ethyl acetate, washed with water and brine and dried over sodium sulfate. After removal of the solvent under reduced pressure, residue was purified by silica gel chromatography (eluent ethyl acetate to methanol) to give 3-(4-hydroxymethylphenyl)-1-methyl-1,2,5,6-tetrahydropyridine (0.63 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504411B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-4a443f0ff195436fbdf1639a06c2e660 |
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| Source note | uspto-grants-2009_03 |
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