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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765709Generated: October 31, 2026

Acetonitrile → 6-Bromo-8-[(cyclopropyl-amino)-methyl]-2,2,4,4-tetramethyl-chroman

https://huagongshe.com/reaction/1765709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantCyclopropylamineHCID 69828—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-Bromo-2,2,4,4-tetramethyl chroman-8-carbaldehydeHCID 22568946—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product6-Bromo-8-[(cyclopropyl-amino)-methyl]-2,2,4,4-tetramethyl-chromanHCID 2110721850%

Reaction Steps

A stirred, cooled (ice bath) solution of 6-bromo-2,2,4,4-tetramethyl chroman-8-carbaldehyde (U.S. Pat. No. 6,252,090, 2.4 g, 8.4 mmol) in dichloromethane (10 mL) and acetonitrile (9 mL) was treated with cyclopropyl amine (1.45 mL, 21 mmol). After 5 minutes, acetic acid (1 mL) was added followed by sodium cyanoborohydride (1.33 g, 21 mmol). The reaction mixture was stirred at ambient temperature for 2 h. The volatiles were distilled off in vacuo, the residue was diluted with water and extracted with ethyl acetate (×2). The combined organic extract was washed with water, saturated aqueous sodium bicarbonate and brine, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to an oil. Flash column chromatography over silica gel (230–400 mesh) afforded the title compound (1.4 g, 50%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226951B2
Source datasetuspto-grants-2007_06
ORD IDord-ed069717ca284564870253a7aeef9d85
Source noteuspto-grants-2007_06