3-O-Benzyl-1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose → 3-O-Benzyl-1,2-O-isopropylidene-alpha-D-glucofuranose

반응식

CC1(C)[O:6][CH:5]([CH:7]2[O:11][CH:10]3[O:12][C:13]([CH3:16])([CH3:15])[O:14][CH:9]3[CH:8]2[O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:4][O:3]1>C(O)(=O)C>[CH3:15][C:13]1([CH3:16])[O:12][C@@H:10]2[C@@H:9]([C@@H:8]([O:17][CH2:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[C@@H:7]([C@H:5]([OH:6])[CH2:4][OH:3])[O:11]2)[O:14]1

참가 물질

실험 절차

Partial hydrolysis of 30B (50 g) was achieved in 75% acetic acid in a period of 20 h. Concentration to a smaller volume and extraction with ethyl acetate yielded 30C, 40 g, (90%). Homogeneous by TLC.

후처리

concentrationConcentration
extractionto a smaller volume and extraction with ethyl acetate

출처 및 근거

ORD 기록: ord-355d52c6a6c149219592af70d0e8c794
출처 데이터셋: uspto-grants-2004_09
DOI: 10.6084/m9.figshare.5104873.v1
특허 번호: US06794499B2

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참가 물질

반응물 1

HCID 979073-O-Benzyl-1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose

생성물 1

HCID 110881883-O-Benzyl-1,2-O-isopropylidene-alpha-D-glucofuranose

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Partial hydrolysis of 30B (50 g) was achieved in 75% acetic acid in a period of 20 h. Concentration to a smaller volume and extraction with ethyl acetate yielded 30C, 40 g, (90%). Homogeneous by TLC.

후처리

concentrationConcentration
extractionto a smaller volume and extraction with ethyl acetate

출처 및 근거

ORD 기록: ord-355d52c6a6c149219592af70d0e8c794
출처 데이터셋: uspto-grants-2004_09
DOI: 10.6084/m9.figshare.5104873.v1
특허 번호: US06794499B2

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불러오는 중…