JCGG ID |
JCGG-RAC0001912 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001912 | |||||||
Regist Date |
2012/06/21 18:14:11 | |||||||
REACTANT | ||||||||
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Mol |
25.6 mmol | |||||||
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Reactant Type |
2-bromethanol | |||||||
Mol |
30.7 mmol | |||||||
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Reactant Type |
BF3*OEt2 | |||||||
Mol |
128 mmol | |||||||
PRODUCT | ||||||||
MOLECULE ID |
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Yield |
60% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
25 minutes + 1 hour, 12 hours | |||||||
Reaction Temp |
0 degree C, room temp | |||||||
Solvent |
dry CH2Cl2, dry CH2Cl2 | |||||||
Comment |
1) +all, 2) temperature change | |||||||
BF3*OEt2 was added dropwise over 25 minutes. | ||||||||
The reaction was conducted in dark condition. | ||||||||
COMMENT | ||||||||
Keywords: synthesis, (2-bromoethyl)2,3,4,6-tetra-O-acetyl-beta-D-glucopyranoside | ||||||||
There are multiple steps in this reaction. | ||||||||
REFERENCE | ||||||||
Reference Id |
REF-0000-000253 | |||||||
Source |
Essentials of Carbohydrate Chemistry and Biochemistry | |||||||
Reference Id |
REF-0000-000254 | |||||||
Source |
ISBN 978-3-527-31528-4 | |||||||
Reference Id |
REF-0000-000289 | |||||||
Source |
Carbohydr. Res. 116, 303 (1983) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |