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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872756Generated: October 30, 2026

Sodium Hypochlorite → 2-chloro-4-(4-chloro-1H-pyrazol-5-yl)benzonitrile

https://huagongshe.com/reaction/872756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HypochloriteHCID 23665760—
Reactant2-chloro-4-(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)benzonitrileHCID 70656253—
SolventAcetic AcidHCID 176—
Product2-chloro-4-(4-chloro-1H-pyrazol-5-yl)benzonitrileHCID 6717250158.4%

Reaction Steps

2-chloro-4-(1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)benzonitrile (12.0 g, 41.7 mmol) was dissolved in acetic acid (20 ml) and sodium hypochlorite solution (29.0 ml, 416 mmol) was added. The reaction mixture was stirred at RT overnight. Further again, acetic acid (120 ml) and sodium hypochlorite solution (14 ml) were added and the mixture was stirred at RT overnight. The precipitate was filtrated and washed with water and DCM. The precipitate was dried in vacuum 40° C. overnight to yield 5.8 grams of 2-chloro-4-(4-chloro-1H-pyrazol-5-yl)benzonitrile. The mixture of 2-chloro-4-(4-chloro-1H-pyrazol-5-yl)benzonitrile (5.8 g, 24.36 mmol) and 10% HCl/ethanol solution (167 ml, 365 mmol) was stirred for 2 h at RT and the precipitate was filtrated and washed with water. The precipitate was silted up with ethanol to yield 4.0 g of the raw material. The product was purified with Flash-chromatography to yield total 18% of the title compound. 1H NMR (400 MHz; d6-DMSO): δ 8.05 (m, 2H), 8.16 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975254B2
Source datasetuspto-grants-2015_03
ORD IDord-f466c12c9c9c43d9afb7823608b67f21
Source noteuspto-grants-2015_03