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Boron trifluoride etherate → HCID 67281057, 화합물

HRID 1694725
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HRID 1694725 반응식
B(F)(F)F.CCOCC.[F:10][C:11]([F:30])([F:29])[C:12]1[CH:28]=[CH:27][C:15]([O:16][CH2:17][C:18]([O:20][CH2:21][C:22]2([CH3:26])[CH2:25][O:24][CH2:23]2)=[O:19])=[CH:14][CH:13]=1>ClCCl>[CH3:23][C:22]12[CH2:25][O:24][C:18]([CH2:17][O:16][C:15]3[CH:27]=[CH:28][C:12]([C:11]([F:30])([F:29])[F:10])=[CH:13][CH:14]=3)([O:19][CH2:26]1)[O:20][CH2:21]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8000Boron trifluoride etherateHCID 86609219[4-(Trifluoromethyl)phenoxy]-acetic acid, (3-methyl-3-oxetanyl)methyl ester

생성물 1

HCID 67281057HCID 67281057, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Boron trifluoride diethyl etherate (1.48 ml) was added to a solution of the product from step (ii) (14.2 g) in dichloromethane at −78° C. The cooling bath was removed, the mixture, stirred for 3 h then triethylamine (6.2 ml) added. The mixture was reduced to half the volume under reduced pressure then filtered. The filtrate was evaporated under reduced pressure then the residue purified by chromatography on silica (pre-eluted with one column volume of neat triethylamine) eluting with dichloromethane, yield 11.1 g.

후처리

  1. customThe cooling bath was removed
  2. additiontriethylamine (6.2 ml) added
  3. filtrationthen filtered
  4. customThe filtrate was evaporated under reduced pressure
  5. customthe residue purified by chromatography on silica (pre-eluted with one column volume of neat triethylamine)
  6. washeluting with dichloromethane, yield 11.1 g

출처 및 근거

ORD 기록
ord-8874e256ae6c4f94aecef261fbcafe04
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158820B2

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