1941
DOI: 10.1021/ie50373a028
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Derivatives of Allylic Chlorides

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Cited by 44 publications
(6 citation statements)
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References 5 publications
(7 reference statements)
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“…Mkthylallyl|Ether (2a): bp 109 °C;jNMR (CC14)1.72 (3 H, s, CH3), 3.75-4.00 (4 H, m, CH2OCH2), 4.7-6.2 (5 H, m, vinyl) 23. Anal.…”
unclassified
“…Mkthylallyl|Ether (2a): bp 109 °C;jNMR (CC14)1.72 (3 H, s, CH3), 3.75-4.00 (4 H, m, CH2OCH2), 4.7-6.2 (5 H, m, vinyl) 23. Anal.…”
unclassified
“…Of greatest commercial significance are its reaction with sodium sulfite to give sodium methallyl sulfonate and the production of 2-methylepichlorohydrin. For further chemical reactions of methallyl chloride, see [142][143][144][145][146].…”
Section: Chemical Propertiesmentioning
confidence: 99%
“…Methallyl chloride and methallyl ether each form an azeotrope with water, which boils at 92° in both cases. Table 344 shows how complicated the separation of methallyl alcohol and methallyl ether is, since the two give azeotropes not only with water but also with one another [24].…”
Section: A) Hydrolysis Of Methallyl Chloride To Methallyl Alcohol Andmentioning
confidence: 99%
“…The pure isobutyraldehyde boils at 64·1° and has a density at 20° of 0*759. Isobutyraldehyde can be readily oxidized with a 95% yield to isobutyric acid [27]. In this way, therefore, isobutyric acid can be obtained from isobutene by chlorination, saponification, isomerization, and oxidation with an over-all yield of 60%.…”
Section: A) Hydrolysis Of Methallyl Chloride To Methallyl Alcohol Andmentioning
confidence: 99%