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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305964Generated: November 1, 2026

Boron tribromide → HCID 18433429, compound

https://huagongshe.com/reaction/2305964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 22728151HCID 22728151—
SolventWaterHCID 962—
ProductHCID 18433429HCID 18433429—

Reaction Steps

N-Cyclobutyl-5-(2,6-dimethyl-4-nitro-phenoxy)-2-hydroxy-N-methyl-benzamide was prepared from N-cyclobutyl-5-(2,6-dimethyl-4-nitro-phenoxy)-2-methoxy-N-methyl-benzamide 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 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.: 370.4, Found: 371.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441015B2
Source datasetuspto-grants-2002_08
ORD IDord-c06604e91acc40abb1c32d870a120a5b
Source noteuspto-grants-2002_08