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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221173Generated: October 30, 2026

Tetrahydrofuran → 7-bromo-9,9-dibutyl-9H-fluoren-2-amine

https://huagongshe.com/reaction/221173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantButyl iodideHCID 10962—
Reactant2-Amino-7-bromofluoreneHCID 23126—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Product7-bromo-9,9-dibutyl-9H-fluoren-2-amineHCID 59325937—

Reaction Conditions

Temperature50 °C

Reaction Steps

Under N2 atmosphere, 0.52 parts of 7-bromo-9H-fluoren-2-ylamine, 2.21 parts of 1-iodobutane, and 1.35 parts of potassium tert-butoxide were added into 20 parts of dry tetrahydrofuran, followed by stirring and mixing. Then, the reaction mixture was heated to 50° C. and reacted for 18 hours. After the reaction mixture was cooled, water was used for quenching the reaction, diethyl ether was used for extracting the product, and magnesium sulfate was used for dehydration. After removing the solvent, the residual was purified with column chromatography method by using dichloromethane/hexane co-solvent as an eluent, to obtain a compound (31) of the present example. This compound was in a form of a brown-yellow solid, and the yield of this compound was 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08203068B2
Source datasetuspto-grants-2012_06
ORD IDord-89097196b2d94d0a974258d8840205f5
Source noteuspto-grants-2012_06