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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289368Generated: October 31, 2026

Benzyl Bromide → HCID 53922389, compound

https://huagongshe.com/reaction/1289368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 53745759HCID 53745759—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDimethylformamideHCID 6228—
ProductHCID 53922389HCID 53922389105.3%

Reaction Steps

A mixture of the title compound of Step D (0.5 g, 2.46 mmol), K2 CO3 (1.02 g, 7.38 mmol), benzyl bromide (0.463 g, 2.71 mmol) and TBAB (79 mg) in DMF (5 mL) was stirred at room temperature for 48 h. After the reaction was complete, the reaction mixture was poured into an H2 O/ethyl acetate mixture (10/100 mL). The organic phase was separated, dried and concentrated to give the title compound of Step E as a brown solid (0.76 g). 1H NMR (CDCl3, 300 MHz): δ7.32 (m,6H, aromatic) 6.72 (d,1H, 11 Hz), 6.34 (d, 1H, 8 Hz), 4.82 (s,2H), 4.69 (s,2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750471
Source datasetuspto-grants-1998_05
ORD IDord-370d93818f034f8eadd573a119d369e1
Source noteuspto-grants-1998_05