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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555429Generated: October 26, 2026

2-Tert-Butylphenol → 2-(2-Tert-butylphenoxy)-3-nitrothiophene

https://huagongshe.com/reaction/555429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tert-ButylphenolHCID 6923—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-3-nitrothiopheneHCID 220186—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-(2-Tert-butylphenoxy)-3-nitrothiopheneHCID 59857371—

Reaction Conditions

Temperature105 °C

Reaction Steps

To a solution of 2-chloro-3-nitrothiophene (1.13 g, 6.93 mmol) in NMP (10 mL) in a pressure vessel was added 2-tert-butylphenol (1.04 g, 6.93 mmol) and K2CO3 (1.0 g, 10.1 mmol). The reaction was flushed with nitrogen, sealed and then heated to 105° C. for 48 h. The reaction was cooled to rt, diluted with EtOAc (˜150 mL) and washed twice with saturated aqueous NaCl (2ט150 mL). The aqueous washes were then back extracted with EtOAc. The combined organics were dried over MgSO4, filtered and concentrated to yield the crude desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053450B2
Source datasetuspto-grants-2011_11
ORD IDord-eb9dfcffa5234e0e81072bfdd967b62b
Source noteuspto-grants-2011_11