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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389467Generated: October 30, 2026

Water → 3-Bromo-2-tert-butylsulfanyl-5-nitro-benzaldehyde

https://huagongshe.com/reaction/389467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-Butyl mercaptanHCID 6387—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-2-fluoro-5-nitrobenzaldehydeHCID 86662401—
SolventDimethylformamideHCID 6228—
Product3-Bromo-2-tert-butylsulfanyl-5-nitro-benzaldehydeHCID 86662400104.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 3-bromo-2-fluoro-5-nitro-benzaldehyde (1.0 g, 4 mmol), potassium carbonate (667 mg, 4.8 mmol) and 2-methyl-2-propanethiol (326 mg, 0.40 mL, 3.6 mmol) in dry DMF (5 mL) was heated at 110° C. in a sealed tube for 16 h. The reaction was cooled to RT, water was added, and the mixture extracted with dichloromethane (2×30 mL). The combined organic fractions were washed with water (3×15 mL), dried over sodium sulfate, filtered and concentrated to afford 1.2 g of the crude title compound, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378104B2
Source datasetuspto-grants-2013_02
ORD IDord-2c4fecd2afb640f0bd8d512cea9bed19
Source noteuspto-grants-2013_02