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Methyl iodide → Butanoic acid, 2-ethyl-2-methyl-, methyl ester

HRID 462351
Notes
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Reaction equation

HRID 462351 reaction equation
[CH2:1]([CH:3]([CH2:8][CH3:9])[C:4]([O:6][CH3:7])=[O:5])[CH3:2].[CH2:10]([Li])CCC.C(NC(C)C)(C)C.CI>>[CH2:1]([C:3]([CH3:10])([CH2:8][CH3:9])[C:4]([O:6][CH3:7])=[O:5])[CH3:2]
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 6328Methyl iodideHCID 7912DiisopropylamineHCID 69951Methyl 2-ethylbutyrateHCID 178418339Butyllithium

Product 1

HCID 521437Butanoic acid, 2-ethyl-2-methyl-, methyl ester

Procedure

A 16.5 Kg portion of methyl 2-ethylbutyrate was reacted with 60 Kg of n-butyl lithium, diisopropylamine, and 19.1 Kg of methyl iodide to provide 17.4 Kg of methyl 2-ethyl-2-methylbutyrate. A 7.5 Kg portion of the ester thus formed was reacted with 3.25 Kg of acetonitrile and 5.03 g of sodium hydride in 33 liters of tetrahydrofuran to provide 1-ethyl-1-methylpropyl cyanomethyl ketone. The ketone thus formed was reacted with 4.35 Kg of hydroxylamine hydrochloride and 2.54 Kg of sodium hydroxide in 44 liters of water to provide 5.65 Kg of 5-amino-3-(1-ethyl-1-methylpropyl)isoxazole.

On this pageParticipantsProcedureSources & evidenceReaction notes

Sources & evidence

ORD record
ord-854e48500d5545af8a757075b171a31b
Source dataset
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04515625

Reaction notes

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