Tetrahydrofuran → tert-butyl 4-[(1S)-1-hydroxyethyl]benzoate

HRID 80571ノート

反応式

HRID 80571 の反応式
[C:1]([C:4]1[CH:16]=[CH:15][C:7]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])=[CH:6][CH:5]=1)(=[O:3])[CH3:2].O1CCCC1.B(Cl)([C@H]1[C@H](C)[C@@H]2C(C)(C)[C@@H](C2)C1)[C@H]1[C@H](C)[C@@H]2C(C)(C)[C@@H](C2)C1.N(CCO)CCO>CCCCCC>[OH:3][C@H:1]([C:4]1[CH:16]=[CH:15][C:7]([C:8]([O:10][C:11]([CH3:13])([CH3:12])[CH3:14])=[O:9])=[CH:6][CH:5]=1)[CH3:2]

参加物

6

反応物 4

HCID 8028TetrahydrofuranHCID 8113DiethanolamineHCID 11131038Chlorobis((1R,2S,3R,5R)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-yl)boraneHCID 13844704tert-Butyl 4-acetylbenzoate

生成物 1

HCID 70815081tert-butyl 4-[(1S)-1-hydroxyethyl]benzoate収率 103.3%

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

実験手順

To tert-butyl 4-acetylbenzoate (3.33 g) in a tetrahydrofuran (23 ml) solution, (−)-B-chlorodiisopinocampheylborane in a 65% hexane solution (11.2 ml) was added dropwise under ice cooling, then the mixture was stirred at that temperature for 1.5 hours. The reaction solution was concentrated, and the residue was diluted by diethyl ether. To the thus solution obtained, diethanolamine (4.3 ml) was added under ice cooling, and the mixture was stirred at room temperature for 2 hours. The precipitates were removed by filtration, and the filtrate was concentrated. The residue was purified by flash column chromatography (silica gel, hexane/ethyl acetate=9/1 to 4/1) to obtain the title compound (3.47 g).

後処理

  1. concentrationThe reaction solution was concentrated
  2. additionthe residue was diluted by diethyl ether
  3. customTo the thus solution obtained
  4. stirringthe mixture was stirred at room temperature for 2 hours
  5. customThe precipitates were removed by filtration
  6. concentrationthe filtrate was concentrated
  7. customThe residue was purified by flash column chromatography (silica gel, hexane/ethyl acetate=9/1 to 4/1)

出典と根拠

ORDレコード
ord-1a363a750112412691c011c2365672b9
出典データセット
uspto-grants-2014_09
特許番号
US08846660B2

反応ノート

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