HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2122039Generated: October 30, 2026
Sodium borohydride → 1-Benzyl-4-methyl-1,2,3,6-tetrahydropyridine
https://huagongshe.com/reaction/2122039
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Pyridinium, 4-methyl-1-(phenylmethyl)-, chloride (1:1) | HCID 10856996 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 1-Benzyl-4-methyl-1,2,3,6-tetrahydropyridine | HCID 6421572 | 100% |
Reaction Steps
To a stirred solution of the product from Method A (38 grams/0.171 mol) dissolved in 140 mL of 10:1 ethanol/water at 0° C. was added 16 grams (0.427 mol) of sodium borohydride portion-wise over 25 minutes. The resulting mixture stirred for 18 hours at room temperature, at which time, the reaction was quenched upon addition of 100 mL of water. The reaction mixture was filtered, the filter cake washed with water and ethylacetate, and the combined filtrates concentrated under reduced pressure to remove the organics. The residue was diluted with water (100 mL) and extracted 3 times with 150 mL with ethylacetate. The combined ethylacetate extracts were dried over Na2SO4 and concentrated to dryness in vacuo affording 32 grams (100%) of the title compound as a yellow oil. LRMS: 188 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06696567B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-127692d30b9844b88dc66002125de2f2 |
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| Source note | uspto-grants-2004_02 |
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