This study has resulted in a route to the first known NHZ functionalized xylenebased crown ether, 5-amino-2-methoxy-1,3-xylyl-18-crown-5. The route involves preparing 5-azido-2-methoxy-1,3-xylyl-18-crown-5 from 5-bromo-2-methoxy-1,3-xylyl18-crown-5 by reacting it in turn with n-BuLi and tosyl azide. 5-Amino-2-methoxy-1,3xylyl-l8-crown-5 was obtained by reducing 5-azido-2-methoxy-1,3-xylyl-l8-crown-5 with aqueous sodium borohydride in the presence of a phase transfer agent. The 'H NMR spectrum of the amino derivative showed NMR signals at 6 3.4-3.7 (crown CHZ), S 4.0 (benzylic), S 4.47 (methoxy), and 6 6.58 (aromatic) ppm. The integrated areas were consistent with the formula, and they also suggested the NH2 protons were in the crown CH2 area. The IR (KBr pellet) spectrum showed bands at 3408 cm' and 3364 cm' corresponding to the N-H asymmetric and symmetric stretches, respectively. This study has also provided a new procedure for the preparation of 4-bromo-2,6-bis(bromomethyl) anisole, which was the intermediate for 5-bromo-2-methoxy-1,3-xylyl-18-crown-5. It involved reacting 4-bromophenol in turn with 30 % formaldehyde, dimethylsulfate, and HBr in acetic acid. / Department of Chemistry
| Identifer | oai:union.ndltd.org:BSU/oai:cardinalscholar.bsu.edu:handle/187707 |
| Date | January 2004 |
| Creators | Yonekawa, Sayuri |
| Contributors | Storhoff, Bruce N. |
| Source Sets | Ball State University |
| Detected Language | English |
| Format | vii, 50 leaves : ill. ; 28 cm. |
| Source | Virtual Press |
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