반응 #2080906

ord-83f563abdf154b2a819c4d9151e50fb3

반응 방정식

CC(=O)O[C@H]1[C@H](OC(C)=O)CSC(Br)[C@@H]1OC(C)=O
2,3,4-tri-O-acetyl-5-thio-D-xylopyranosyl bromide
Oc1cccc2ccoc12
7-hydroxybenzofuran
→
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1cccc2ccoc12
desired product
수율 14.0%
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1cccc2ccoc12
7-benzofuranyl 2,3,4-tri-O-acetyl-5-thio-β-D-xylopyranoside
수율 14.0%

반응물

CC(=O)O[C@H]1[C@H](OC(C)=O)CSC(Br)[C@@H]1OC(C)=O
2,3,4-tri-O-acetyl-5-thio-D-xylopyranosyl bromide
Oc1cccc2ccoc12
7-hydroxybenzofuran

시약

없음

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

By carrying out the process in a manner similar to example 7, starting from 2,3,4-tri-O-acetyl-5-thio-D-xylopyranosyl bromide and 7-hydroxybenzofuran, the desired product is obtained in the form of a white solid with a yield of 14%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07652032B2uspto-grants-2010_01