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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52264Generated: October 28, 2026

Chloroform → HCID 53934247, compound

https://huagongshe.com/reaction/52264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantBoron tribromideHCID 25134—
ReactantHCID 70145878HCID 70145878—
SolventDichloromethaneHCID 6344—
ProductHCID 53934247HCID 5393424797%

Reaction Conditions

Temperature-40 °C

Reaction Steps

(R)-8-Fluoro-3-(N-isopropyl-N-propylamino)-5-methoxy-3,4-dihydro-2H-1-benzopyran hydrochloride (1.03 g, 3.24 mmol) was dissolved in anhydrous CH2Cl2 (30 mL) and cooled to -40° C. To the solution was BBr3 (0.77 mL, 8.1 mmol), dissolved in anhydrous CH2Cl2 (5 mL), added dropwise. The cooling-bath was removed and after 3 h at room temperature the reaction was complete. The reaction was poured out onto an ice/2M NH3 solution and the mixture was extracted, twice, with diethyl ether. The combined ether portions were treated with brine, dried (Na2SO4), filtered, and the solvent removed in vacuo to give the crude residue. Chromatography on silica (eluent: 20% ethyl acetate/hexane) gave 0.84 g (97% yield) of the title compound as a clear oil [α]21D =-94.2° (C=0.1 CHCl3) GC-MS (70 eV) M=267 (26%). The hydrochloride salt was made by dissolving the pure base in diethyl ether and dropping an excess of an ethereal HCl solution. The salt was recrystallized from CHCl3 /diethyl ether/ethyl acetate to give a white solid. Mp: 220°-2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616610
Source datasetuspto-grants-1997_04
ORD IDord-4c754d08108a4c85ab10a370bb40a840
Source noteuspto-grants-1997_04