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Me-bpe, (R,R)- → Methyl 6-Methoxy-2,3-dihydrobenzofuran-3-acetate

HRID 1908920
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HRID 1908920 반응식
C[C@H]1P(CCP2[C@H](C)CC[C@H]2C)[C@H](C)CC1.[CH3:17][O:18][C:19]1[CH:32]=[CH:31][C:22]2[C:23]([CH2:26][C:27]([O:29][CH3:30])=[O:28])=[CH:24][O:25][C:21]=2[CH:20]=1.[H][H]>CO>[CH3:17][O:18][C:19]1[CH:32]=[CH:31][C:22]2[CH:23]([CH2:26][C:27]([O:29][CH3:30])=[O:28])[CH2:24][O:25][C:21]=2[CH:20]=1
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참가 물질

5

반응물 3

HCID 2734555Me-bpe, (R,R)-HCID 15618717Methyl 2-(6-methoxy-1-benzofuran-3-yl)acetateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 59342592Methyl 6-Methoxy-2,3-dihydrobenzofuran-3-acetate수율 24.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a mixture of (1,5-cyclooctadiene)rhodium trifluoromethanesulfonate (12 mg) and (R,R)-Me-BPE (6.5 mg) was added methanol (2.5 mL) sufficiently substituted by argon gas, and the mixture was stirred at room temperature for 15 min. This was added to methyl (6-methoxy-1-benzofuran-3-yl)acetate (55 mg), and the mixture was stirred at 70° C. for 3 hr under 0.7 MPa hydrogen atmosphere. The reaction mixture was quantified by HPLC. As a result, the enantiomeric excess was 52.8%, and the yield was 24.3%.

출처 및 근거

ORD 기록
ord-aabb859dacfb423f9fd624d1ec3ff196
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08598226B2

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