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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846023Generated: November 3, 2026

2-Bromopropane → HCID 86723246, compound

https://huagongshe.com/reaction/1846023

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium AcetateHCID 517045—
Reactant4-Bromo-3-fluorobenzenesulfonyl chlorideHCID 2778218—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86723246HCID 8672324612%

Reaction Steps

To a solution of 4-bromo-3-fluorobenzene-1-sulfonyl chloride (5.40 mL, 36.5 mmol) in THF (150 mL) at 0° C. was added hydrazine monohydrate (6.20 mL, 63.9 mmol) dropwise under a nitrogen atmosphere. The reaction mixture was stirred for 1.5 hours. The solvent was removed in vacuo and replaced with heptanes (150 mL) and the resulting precipitate was collected by filtration. The solid was dissolved in industrial methylated spirit (150 mL) and to this solution was added sodium acetate (17.9 g, 218 mmol) and 2-bromopropane (17.2 mL, 183 mmol). The resultant reaction mixture was stirred at 85° C. for 16 hours under a nitrogen atmosphere. The reaction mixture was cooled to room temperature and quenched with water (300 mL) before being extracted with CH2Cl2 (3×300 mL). The combined organic extracts were washed with brine (300 mL), dried over MgSO4, filtered and evaporated in vacuo. The crude material was purified by silica gel column chromatography eluting with EtOAc:heptanes 20/80 to afford title compound as a colourless solid in 12% yield, 1.19 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952008B2
Source datasetuspto-grants-2015_02
ORD IDord-04e602a484734e43a5a012eca7081169
Source noteuspto-grants-2015_02