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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304918Generated: November 1, 2026

Iodine → HCID 23512834, compound

https://huagongshe.com/reaction/2304918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23512846HCID 23512846—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23512834HCID 2351283423%

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C., a solution of of 4-(4-chlorophenyl)-N-methylbutyramide (3.80 g, 18.0 mmol) in tetrahydrofuran (60 ml) was added to a suspension of sodium borohydride (1.60 g, 43.1 mmol) in THF (60 ml). The mixture was stirred for 20 min at 0° C. A solution of iodine (4.6 g, 18.0 mmol) in THF (100 ml) was added dropwise. After the addition was finished, the reaction mixture was warmed to 70° C. It was stirred for 16 hours at this temperature. It was cooled to 0° C. Methanol (100 ml) was added dropwise. The solvents were removed in vacuo. The residue was dissolved in a 20% aqueous solution of sodium hydroxide (160 ml) and tert-butyl methyl ether (200 ml). The phases were separated. The aqueous phase was extracted with tert-butyl methyl ether (3×70 ml). The combined organic layers were dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (90 g), using DCM/methanol/25% aqueous ammonia as eluent, to give 820 mg of N-[4-(4-chlorophenyl)butyl]-N-methylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437147B1
Source datasetuspto-grants-2002_08
ORD IDord-6ceb6c01435744528cc93bbaabd4decc
Source noteuspto-grants-2002_08