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Methyl iodide → 9-Methylfluorene

HRID 871190
Notes
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Reaction equation

HRID 871190 reaction equation
[CH:1]1[C:13]2[CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.[Li][CH2:15]CCC.IC.OC1O[C@@H](CO)[C@H](O)[C@H](O)[C@H]1O>>[CH3:15][CH:12]1[C:11]2[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=2[C:5]2[C:13]1=[CH:1][CH:2]=[CH:3][CH:4]=2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 6328Methyl iodideHCID 6853FluoreneHCID 10219674L-AltroseHCID 178418339Butyllithium

Product 1

HCID 172999-Methylfluorene

Procedure

Fluorene (15.0 g, 90.4 mmol), n-BuLi (48.1 ml, 120 mmol, 2.5 M in hexane), RX=iodomethane (19.3 g, 136 mmol). 40 was isolated as a yellowish waxy solid (16.2 g, quant.). The analytical data were identical to those in the literature (M. A. Schmidt, H. G. Alt, W. Milius, J. Organomet. Chem. 1996, 525, 15).

Workup

  1. custom40 was isolated as a yellowish waxy solid (16.2 g, quant.)

Sources & evidence

ORD record
ord-16ef402a9e8c4625a31f3739f3773ba0
Source dataset
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08969624B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes