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Propylene Oxide → 3-((s)-2-Hydroxypropylthio)phenylboronic acid

HRID 2262065
ノート
印刷プレビュー

反応式

HRID 2262065 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6378Propylene OxideHCID 27739223-Mercaptophenylboronic AcidHCID 9989226Alumina

生成物 1

HCID 671904283-((s)-2-Hydroxypropylthio)phenylboronic acid収率 90%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-ed30a94fad9c48f794b59b6d2355b70e
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07846929B2

反応ノート

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