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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38446Generated: October 29, 2026

Benzyl Bromide → HCID 59226034, compound

https://huagongshe.com/reaction/38446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant6-Fluoro-7-methylisoquinolin-1(2H)-oneHCID 59226050—
CatalystHCID 178418647HCID 178418647—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59226034HCID 5922603415.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

6-Fluoro-7-methyl-2H-isoquinolin-1-one (prepared as described in WO2007012421, 13.2 g, mmol) was dissolved in tetrahydrofurane (175 mL). After addition of silver carbonate (41.2 g), benzyl bromide (15.3 g) was added dropwise. The mixture was stirred overnight. The mixture was heated to 70° C. and another 3 mL of benzyl bromide were added. Heating was continued until no further conversion was observed. The mixture was taken up in ethyl acetate, filtered over celite, evaporated and the residue was taken up in little ethyl acetate. The formed precipitate was filtered off to give 3.0 g of (2). The mother liquor was concentrated and chromatographed on silica gel to yield another 8.6 g of (2). Rt=4.00 min (Method 2). Detected mass: 268.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524737B2
Source datasetuspto-grants-2013_09
ORD IDord-87f707211df34d2d8cfc817ce3ac0921
Source noteuspto-grants-2013_09