2-formyl-6-methoxyphenyl oleate

DOI: 10.14469/hpc/10233 Metadata

Created: 2022-03-13 04:24

Last modified: 2022-03-13 12:14

Author: Siran Shuai

License: Creative Commons: Public Domain Dedication 1.0

Funding: (none given)

Description

DMAP (0.06 g, 0.5 mmol) was mixed with EDC.HCl (1.25 g, 6.5 mmol) in acetonitrile (25 mL), added with ortho-vanillin and oleic acid. The mixture was heated under reflux for one hour and was monitored by TLC. It was extracted with haxane and ethyl acetate. The resulting product was then washed with 1 M aqueous HCl twice, aqueous NaHCO3 twice, water and NaCl twice. MgSO4 was added to dry it and and the solvent was removed with rotary evaporator. Finally 2-formyl-6-methoxyphenyl oleate was formed.

Files

FilenameSizeTypeDescription
2-formyl-6-methoxyphenyl oleate.cdxml 7KB chemical/x-cdxml chemdraw file
ss5121.mnova 482KB chemical/x-mnova MestreNova data file
ss5121.mnpub 0 chemical/x-mnpub Mestrenova signature file for ss5121.mnova
ss5121.jdx 155KB chemical/x-jcamp-dx jdx data file
ss5121_PROTON.pdf 383KB application/pdf pdf data file
ss5121_PROTON-1-1.jdf 550KB chemical/x-jeol-jdf jdf data file
ss5121_PROTON-1-1.mnpub 0 chemical/x-mnpub Mestrenova signature file for ss5121_PROTON-1-1.jdf

Member of collection / collaboration

DOIDescription
10.14469/hpc/8679 1st Year undergraduate synthesis 1.2 laboratory (2021-2022)

Subject Keywords

KeywordValue
inchi InChI=1S/C26H40O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21-25(28)30-26-23(22-27)19-18-20-24(26)29-2/h10-11,18-20,22H,3-9,12-17,21H2,1-2H3/b11-10-
inchikey UJCBTNJTWLPTOX-KHPPLWFESA-N

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