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Ethylenediamine → (1S)-1-(2-Hydroxyethyl)-3,4-dihydro-1H-2-benzopyran-6-carbonitrile

HRID 2056722
ノート
印刷プレビュー

反応式

HRID 2056722 の反応式
Br[C:2]1[CH:3]=[CH:4][C:5]2[C@H:10]([CH2:11][CH2:12][OH:13])[O:9][CH2:8][CH2:7][C:6]=2[CH:14]=1.[Cu][C:16]#[N:17].C(N)CN>CN(C=O)C.[Cu]I>[OH:13][CH2:12][CH2:11][C@H:10]1[C:5]2[CH:4]=[CH:3][C:2]([C:16]#[N:17])=[CH:14][C:6]=2[CH2:7][CH2:8][O:9]1
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

6

反応物 3

HCID 3301EthylenediamineHCID 536878432-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)ethanolHCID 178418546HCID 178418546、化合物

生成物 1

HCID 69306499(1S)-1-(2-Hydroxyethyl)-3,4-dihydro-1H-2-benzopyran-6-carbonitrile

試薬・触媒・溶媒 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒
HCID 6228
Dimethylformamide
溶媒

反応条件

温度
140 °C

実験手順

A suspension of 2-((1S)-6-bromo-3,4-dihydro-1H-2-benzopyran-1-yl)ethanol (300 g, 1.17 mol), copper(I) cyanide (209 g, 2.34 mol), and copper(I) iodide (33.3 g, 0.18 mol) in dry DMF (1.16 L), under an atmosphere of nitrogen, was heated to 140° C. After 8 h at this temperature, HPLC analysis of an aliquot indicated that the reaction was complete. The reaction mixture was cooled to room temperature and poured into an aqueous solution of ethylenediamine (3 L, v/v 3/1) then extracted into toluene. The combined organic layers were washed with water and concentrated in vacuo to give the crude title compound. This material is used without further purification in the subsequent step.

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. extractionthen extracted into toluene
  3. washThe combined organic layers were washed with water
  4. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-1f48a1f58210433eac5430ccd496ee52
出典データセット
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07335660B2

反応ノート

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