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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683986Generated: October 25, 2026

Hydrochloric Acid → HCID 54300597, compound

https://huagongshe.com/reaction/1683986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactantmethyl 2-(5-methoxy-2-methyl-1H-indol-3-yl)acetateHCID 82067—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTetrahydrofuranHCID 8028—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductHCID 54300597HCID 5430059748%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ester from Step 1 (13.8 g, 59 mmol) in THF (300 mL) and DMPU (40 mL) at -78° C. was added KHMDS solution (0.64M/toluene, 95 mL, 60 mmol). The reaction mixture was warmed to 0° C. and was then recooled to -78° C., at which point a solution of 4-bromobenzyl bromide (17.0 g, 68 mmol) in THF (80 mL) was added via double-tipped needle. The reaction was allowed to warm to r.t., and was then poured into 1M HCl (500 mL). The product was extracted with Et2O and the organic phase was washed with H2O and brine. After drying (MgSO4), filtration, and removal of solvent, the crude product was purified by flash chromatography (1:20 EtOAc/toluene). The resulting prodeuct was recrystallized from CH2Cl2 /hexane to give 11.4 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639780
Source datasetuspto-grants-1997_06
ORD IDord-5d03c8c0fcdc4883b2d09df3cd31c2d3
Source noteuspto-grants-1997_06