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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Propylene Oxide → 3-((s)-2-Hydroxypropylthio)phenylboronic acid

HRID 2262065
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인쇄 미리보기

반응식

HRID 2262065 반응식
[CH2:1]1[O:4][CH:2]1[CH3:3].[SH:5][C:6]1[CH:7]=[C:8]([B:12]([OH:14])[OH:13])[CH:9]=[CH:10][CH:11]=1.[O-2].[Al+3].[O-2].[O-2].[Al+3]>C(OCC)C>[OH:4][C@@H:2]([CH3:3])[CH2:1][S:5][C:6]1[CH:7]=[C:8]([B:12]([OH:14])[OH:13])[CH:9]=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6378Propylene OxideHCID 27739223-Mercaptophenylboronic AcidHCID 9989226Alumina

생성물 1

HCID 671904283-((s)-2-Hydroxypropylthio)phenylboronic acid수율 90%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

S-(−) Propylene oxide (152 μL) was added to a mixture of 500 mg of 3-mercaptophenylboronic acid and aluminum oxide (˜30 eq, neutral, activated, ˜150 mesh) in diethyl ether at room temperature. The reaction was monitored by LC/MS until complete. The reaction mixture was evaporated, and then added 1N HCl. The resulting mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over MgSO4, filtered and evaporated to give 3-((S)-2-hydroxypropylthio)phenylboronic acid (414 mg, 90%). The crude product was directly used for next step reaction without purification.

후처리

  1. customThe reaction mixture was evaporated
  2. additionadded 1N HCl
  3. extractionThe resulting mixture was extracted with ethyl acetate (3×50 mL)
  4. dry with materialThe combined organic layers were dried over MgSO4
  5. filtrationfiltered
  6. customevaporated

출처 및 근거

ORD 기록
ord-ed30a94fad9c48f794b59b6d2355b70e
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07846929B2

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