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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantPyridinium, 4-methyl-1-(phenylmethyl)-, chloride (1:1)HCID 10856996—
SolventWater ethanolHCID 19096565—
Product1-Benzyl-4-methyl-1,2,3,6-tetrahydropyridineHCID 6421572100%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696567B2
Source datasetuspto-grants-2004_02
ORD IDord-127692d30b9844b88dc66002125de2f2
Source noteuspto-grants-2004_02