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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670070Generated: November 2, 2026

Diethyl Ether → N-Benzyl-3-hydroxy-5-iodo-benzamide

https://huagongshe.com/reaction/1670070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBoron tribromideHCID 25134—
ReactantN-benzyl-3-iodo-5-methoxy-benzamideHCID 57905830—
SolventDichloromethaneHCID 6344—
SolventAcetone cardiceHCID 18522661—
ProductN-Benzyl-3-hydroxy-5-iodo-benzamideHCID 57905909—

Reaction Steps

A solution of N-benzyl-3-iodo-5-methoxy-benzamide (4.7 g) in anhydrous dichloromethane (100 mL) was cooled to −78° C. in dry ice/acetone bath under flow of argon and a BBr3 solution (38.4 mL of 1 M solution in dichloromethane) was added dropwise. After the addition was completed, the reaction mixture was stirred at room temperature overnight. The reaction mixture was cooled in an ice bath and then quenched by a dropwise addition of methanol. Then it was diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate and concentrated to remove the solvents. The title compound was obtained by trituration with diethyl ether and hexanes (4.1 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989454B2
Source datasetuspto-grants-2011_08
ORD IDord-3374d53e150c4a28b06d3cf01f46ad1e
Source noteuspto-grants-2011_08