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Toluene → HCID 86722663、化合物

HRID 1480437
ノート
印刷プレビュー

反応式

HRID 1480437 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([CH2:10][OH:11])[CH:9]=1)[C:5]#[N:6].[C:12](Cl)([Cl:14])=[O:13].C1(C)C=CC=CC=1>C1COCC1>[C:12]([Cl:14])(=[O:13])[O:11][CH2:10][C:8]1[CH:7]=[C:4]([C:5]#[N:6])[CH:3]=[C:2]([Cl:1])[CH: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

5

反応物 3

HCID 1140TolueneHCID 6371PhosgeneHCID 583695423-Chloro-5-(hydroxymethyl)benzonitrile

生成物 1

HCID 86722663HCID 86722663、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
10 °C

実験手順

3-Chloro-5-(hydroxymethyl)benzonitrile (25 g, 145 mmol) was dissolved in THF (200 mL). The resulting yellow solution was cooled to 10° C. in an ice bath and treated dropwise with phosgene in toluene (152 mL, 289 mmol). The reaction mixture was stirred at ambient temperature for 16 hrs. The mixture was concentrated under reduced pressure and the crude material was diluted with toluene (200 ml) and re-concentrated under reduced pressure. The residue was purified by chromatography on silica (Redisep 340 g column on a Biotage system), eluting with EtOAc/iso-hexane to give 3-chloro-5-cyanobenzyl carbonochloridate as an oil.

後処理

  1. concentrationThe mixture was concentrated under reduced pressure
  2. additionthe crude material was diluted with toluene (200 ml)
  3. concentrationre-concentrated under reduced pressure
  4. customThe residue was purified by chromatography on silica (Redisep 340 g column on a Biotage system),
  5. washeluting with EtOAc/iso-hexane

出典と根拠

ORDレコード
ord-1e8db2fd8a414b3f82f804189bc1cab9
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409895B2

反応ノート

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