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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-Decynoic acid → Dec-3-enoic acid

HRID 1073580
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인쇄 미리보기

반응식

HRID 1073580 반응식
[C:1]([OH:12])(=[O:11])[CH2:2][C:3]#[C:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]>CO.B#[Ni]>[C:1]([OH:12])(=[O:11])[CH2:2][CH:3]=[CH:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 5493723-Decynoic acid

생성물 1

HCID 85855Dec-3-enoic acid

시약·촉매·용매 2

HCID 82791nickel boride (NiB)촉매HCID 887Methanol용매

실험 절차

To 4.5 g (27 mmol) of 3-decynoic acid from Example 30 dissolved in methanol in a Paar bottle is added 2 mg of nickel boride as catalyst. The bottle is flushed with hydrogen, sealed and pressurized with H2 at 2 pounds per square inch. The hydrogenation is allowed to proceed at room temperature for 2 hours. The methanol is stripped in vacuo and the residue is partitioned between ethyl acetate and in HCl. The ethyl acetate layer is separated, dried, (Na2SO4) and is stripped to afford an almost quantitative yield of 3-decenoic acid.

후처리

  1. customThe bottle is flushed with hydrogen
  2. customsealed
  3. customthe residue is partitioned between ethyl acetate and in HCl
  4. customThe ethyl acetate layer is separated
  5. customdried

출처 및 근거

ORD 기록
ord-833a86c7a80647bdaffe07708abbad28
출처 데이터셋
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04970229

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