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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52259Generated: October 28, 2026

Benzyl Bromide → HCID 54247483, compound

https://huagongshe.com/reaction/52259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant(3R)-8-bromo-5-methoxychroman-3-amineHCID 22871216—
SolventAcetonitrileHCID 6342—
ProductHCID 54247483HCID 54247483155.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

(R)-3-Amino-8-bromo-5-methoxy-3,4-dihydro-2H-1-benzopyran (11.5 g, 44 mmol) was dissolved in 400 mL anhydrous acetonitrile and to the reaction were benzyl bromide (13 mL, 110 mmol), anhydrous potassium carbonate (grounded) (16 g, 116 mmol), and a catalytic amount of KI added and then heated to 85° C. for 48 h. The solvent was removed in vacuo, the remains were taken into a 2M solution of NH3 and then extracted twice with ether. The combined ether portions were treated with brine, dried (MgSO4), filtered, and the solvent removed in vacuo to give the crude residue. Chromatography on silica (eluent: CH2Cl2) gave 15 g (78% yield) of the title compound as a clear oil. [α]21D =-15.5° (C=0.1 CHCl3) GC-MS (70eV) M=437 (15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616610
Source datasetuspto-grants-1997_04
ORD IDord-e26526080f754ba2a9e1f28760042046
Source noteuspto-grants-1997_04