Dimethyl Sulfide → (3,4-Dihydro-2H-1,4-benzoxazin-8-yl)methanol

HRID 1438602ノート

反応式

HRID 1438602 の反応式
O=[C:2]1[NH:7][C:6]2[CH:8]=[CH:9][CH:10]=[C:11]([C:12](O)=[O:13])[C:5]=2[O:4][CH2:3]1.S(C)C.[NH4+].[Cl-]>C1COCC1>[O:4]1[C:5]2[C:11]([CH2:12][OH:13])=[CH:10][CH:9]=[CH:8][C:6]=2[NH:7][CH2:2][CH2:3]1

参加物

5

反応物 3

HCID 1068Dimethyl SulfideHCID 25517Ammonium ChlorideHCID 183549413-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carboxylic acid

生成物 1

HCID 53414296(3,4-Dihydro-2H-1,4-benzoxazin-8-yl)methanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a suspension of 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid (1.51 g, 7.8 mmol) in anhydrous THF (10 mL) was added BH3.Me2S (2 M in THF, 10 mL, 20 mmol) dropwise under nitrogen at 0° C. The resulted mixture was allowed to rise to r.t., and the reaction was continued to be carried out at this temperature overnight. Then, saturated aqueous NH4Cl (30 mL) was added in, and the resulted mixture was extracted with EtOAc (200 mL×2). The combined organic layers were washed with saturated aqueous NaHCO3 solution (30 mL), brine (30 mL), dried (Na2SO4) and filtered before it was concentrated under reduced pressure. The resulted crude product (3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-methanol, which was utilized in the following step without further purification. MS m/z: 166.2 (M+H)+.

後処理

  1. additionwas added BH3
  2. customat 0° C
  3. customto rise to r.t.
  4. customto be carried out at this temperature overnight
  5. extractionwas extracted with EtOAc (200 mL×2)
  6. washThe combined organic layers were washed with saturated aqueous NaHCO3 solution (30 mL), brine (30 mL)
  7. dry with materialdried (Na2SO4)
  8. filtrationfiltered before it
  9. concentrationwas concentrated under reduced pressure

出典と根拠

ORDレコード
ord-39d8c3010cf24e16bfe34e284aaa6fe4
出典データセット
uspto-grants-2009_11
特許番号
US07622583B2

反応ノート

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