3-Buten-1-ol is employed in a study of the Mn-catalyzed hydrohydrazination of olefins. Also used in a study of the conversion of propargylic acetates to ethers catalyzed by ferric chloride.
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Applications
3-Buten-1-ol is employed in a study of the Mn-catalyzed hydrohydrazination of olefins. Also used in a study of the conversion of propargylic acetates to ethers catalyzed by ferric chloride.
Solubility
Soluble in water.
Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only
Francisco Caturla.; Carmen Najera. Preparation and synthetic applications of lithiated vinyl sulfones derived from 3-buten-1-ol and 4-penten-1-ol. Tetrahedron. 1997, 53, (33), 11449-11464.
Naoki Yamamoto.; Satoshi Sato.; Ryoji Takahashi.; Kanichiro Inui. Synthesis of 3-buten-1-ol from 1,4-butanediol over ZrO2 catalyst. Journal of Molecular Catalysis A: Chemical. 2006, 243, (1), 52-59.
Can be used to protect enolizable and base-sensitive carboxylic acids as their 3-butenyl esters which can be cleaved by ozonolysis, followed by treatment with DBU or triethylamine: Tetrahedron Lett., 30, 7317 (1989).