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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272064Generated: November 1, 2026

Boron tribromide → HCID 18456631, compound

https://huagongshe.com/reaction/1272064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 21776239HCID 21776239—
SolventDichloromethaneHCID 6344—
ProductHCID 18456631HCID 1845663142.3%

Reaction Steps

To a solution of 2-(4-methoxy-phenyl)-N-methyl-2-oxo-acetamide (74a) (1.35 g, 6.99 mmol) in 25 mL of CH2Cl2 was added 1.0 M BBr3 in CH2Cl2 (14 mL, 28.0 mmol) at 0° C. The mixture was stirred at 0° C. to room temperature for two hours. The reaction was quenched with MeOH, neutralized with concentrated aqueous NH4OH to pH ˜7. The resulting mixture was stirred at room temperature for one hour. Water was added, and the mixture was extracted with CH2Cl2. The organic phase was dried over Na2SO4, concentrated, and purified by flash column chromatography eluting with 1:1 EtOAc and hexanes to provide 0.53 g off-white solid as the intermediate 74b. 1H NMR (300 MHz, CD3OD) δ 7.03 (d, 2H, J=8.86 Hz), 6.75 (d, 2H, J=8.86 Hz), 2.76 (s, 3H). LCMS (ESI+) [M+Na]/z Calc'd 202, found 202.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208500B2
Source datasetuspto-grants-2007_04
ORD IDord-35010ce1e304411aa7a01652e4d6e07e
Source noteuspto-grants-2007_04