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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305959Generated: November 2, 2026

Boron tribromide → HCID 18433431, compound

https://huagongshe.com/reaction/2305959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 18433435HCID 18433435—
SolventWaterHCID 962—
ProductHCID 18433431HCID 18433431—

Reaction Steps

3,5-Dichloro-4-[4-hydroxy-3-(piperidine-1-carbonyl)-phenoxy]-benzonitrile was prepared from 3,5-dichloro-4-[4-methoxy-3-(piperidine-1-carbonyl)-phenoxy]-benzonitrile according to a procedure analogous to that described in EXAMPLE 2, Step B. Boron tribromide (1M in dichloromethane, 2.0 equiv) was used. After water addition, the mixture was stirred for 30 minutes at RT, then basified with aqueous saturated sodium bicarbonate solution, and extracted with dichloromethane (3×10 ml). The combined organic phases were dried over anhydrous Na2SO4, filtered, and concentrated. The title product of Step E was used in the next step without purification.) MS (APCI+) Calc.: 390.0, Found: 391.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441015B2
Source datasetuspto-grants-2002_08
ORD IDord-8cf00e58410a4440b6523168f8ace387
Source noteuspto-grants-2002_08