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Phenolate Sodium → Carbonate Ion

HRID 14418
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HRID 14418 반응식
[O-:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Na+].[C:9](=[O:13])([O-:12])[O:10]C.C(=O)(OCC)OC/C=C/C1C=CC=CC=1>CCOCC>[O-:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:9](=[O:10])([O-:13])[O-:12]
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참가 물질

6

반응물 3

HCID 4445035Phenolate SodiumHCID 4585885MethylcarbonateHCID 5355242Cinnamyl ethyl carbonate

생성물 2

HCID 19660Carbonate IonHCID 119047Phenolate

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Alkali metal phenoxides as nucleophiles proved to be superior to the combination of phenol and amine base. Sodium phenoxide furnished the corresponding allylation product with high regio- and enantioselectivity (Table 6, entries 4-6). Reaction of sodium phenoxide with methyl carbonate 1a formed the alkylation product at room temperature in a modest 40% yield because of competing trans-esterification (entry 4), but reactions with the more hindered and less reactive (E)-cinnamyl ethyl carbonate (1b of Table 6) occurred without significant competing transesterification. This combination of phenoxide and carbonate gave the branched ether in good yields with excellent regio- and enantioselectivities after 35 h at room temperature or 17 h at 50° C. (Table 6, entries 5 and 6).

후처리

  1. customformed the alkylation product at room temperature in a modest 40% yield because

출처 및 근거

ORD 기록
ord-480284fbc3204e66b6bd04bdf6bcd8f1
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07732365B2

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