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Water → 5-Trifluoromethyl-indan-2-yl-methanol

HRID 1993878
ノート
印刷プレビュー

反応式

HRID 1993878 の反応式
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[CH2:8][CH:7]([C:12](O)=[O:13])[CH2:6]2.B.O>C1COCC1>[F:1][C:2]([F:15])([F:16])[C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[CH2:8][CH:7]([CH2:12][OH:13])[CH2:6]2
参加物反応条件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 962WaterHCID 6331BoraneHCID 668775351H-Indene-2-carboxylic acid, 2,3-dihydro-5-(trifluoromethyl)-

生成物 1

HCID 668775125-Trifluoromethyl-indan-2-yl-methanol収率 101.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

The above 5-trifluoromethyl-indan-2-carboxylic acid (1.03 g, 4.47 mmol) was dissolved in THF (25 mL) and cooled to 0° C. To this solution was added a solution of borane in THF (1M, 6.5 mL). The mixture was warmed to room temperature and stirred for 1 hr. The mixture was treated with water (5 mL) and solvents were evaporated. The residue was extracted with ether and hydrochloric acid (1M). The organic phase was washed with brine and sodium bicarbonate solution. The ether solution was dried and solvents were evaporated to give oily material as 5-trifluoromethyl-indan-2-yl-methanol (0.98 g).

後処理

  1. temperatureThe mixture was warmed to room temperature
  2. customwere evaporated
  3. extractionThe residue was extracted with ether and hydrochloric acid (1M)
  4. washThe organic phase was washed with brine and sodium bicarbonate solution
  5. dry with materialThe ether solution was dried
  6. customsolvents were evaporated

出典と根拠

ORDレコード
ord-fdad3ff1ca1b4aeab707bd15f25a1d48
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07652053B2

反応ノート

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