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Boron trifluoride etherate → 3-(Tetrahydropyran-2-ylthio)-2-methylpropanoic acid

HRID 2419449
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인쇄 미리보기

반응식

HRID 2419449 반응식
[SH:1][CH2:2][CH:3]([CH3:7])[C:4]([OH:6])=[O:5].[O:8]1[CH:13]=[CH:12][CH2:11][CH2:10][CH2:9]1.B(F)(F)F.CCOCC.C(=O)([O-])[O-].[K+].[K+]>C1C=CC=CC=1>[O:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH:9]1[S:1][CH2:2][CH:3]([CH3:7])[C:4]([OH:6])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8000Boron trifluoride etherateHCID 80803,4-dihydro-2H-pyranHCID 11430Potassium CarbonateHCID 1529103-Mercaptoisobutyric acid

생성물 1

HCID 213191383-(Tetrahydropyran-2-ylthio)-2-methylpropanoic acid

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

To a solution of 3-mercapto-2-methylpropanoic acid (2.4 g.) and freshly distillled 2,3-dihydro-4H-pyrane (1.9 g.) in benzene (60 ml.), boron trifluoride etherate (2.8 g.) is added. After two hours, potassium carbonate (4 g.) is added, the mixture is stirred and filtered. The filtrate is concentrated to dryness to yield 3-(tetrahydropyran-2-ylthio)-2-methylpropanoic acid.

후처리

  1. filtrationfiltered
  2. concentrationThe filtrate is concentrated to dryness

출처 및 근거

ORD 기록
ord-cf192b03bd9847c788456f18f38cb8e9
출처 데이터셋
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04105776

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