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(3,4-Dichlorophenyl)acetonitrile → HCID 16079683、化合物

HRID 718119
ノート
印刷プレビュー

反応式

HRID 718119 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]#[N:11])[CH:5]=[CH:6][C:7]=1[Cl:8].[CH2:12]([C@H:14]1[O:16][CH2:15]1)Cl.C[Si]([N-][Si](C)(C)C)(C)C.[Na+]>O1CCCC1>[NH2:11][CH2:10][C@:9]1([C:4]2[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([Cl:1])[CH:3]=2)[CH2:12][C@@H:14]1[CH2:15][OH:16]
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 76690(3,4-Dichlorophenyl)acetonitrileHCID 149428(+)-EpichlorohydrinHCID 2724254Sodium bis(trimethylsilyl)amide

生成物 1

HCID 16079683HCID 16079683、化合物収率 100%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-15 °C

実験手順

To a solution of 2-(3,4-Dichlorophenyl)acetonitrile (3.5 g, 18.81 mmol) and (S)-(+)-Epichlorohydrin (1.877 ml, 23.99 mmol) in tetrahydrofuran (18.5 mL) at −15° C. (dry ice/ethanol/water bath, internal temp monitored with thermocouple) under atmosphere of N2 was added sodium bis(trimethylsilyl)amide (16.5 mL, 33.0 mmol) dropwise over 3 hours. The reaction mixture was stirred for additional 3 hours at −15° C., then, overnight at 4° C. (cold room). The mixture was cooled to −5° C. and borane-methyl sulfide complex (4.4 mL, 44.0 mmol) was added over 2 hours via syringe pump. The reaction mixture was then gradually warmed to 40° C. over 3 hours. After aging 1.5 hours at 40° C., the reaction mixture was cooled to 20-25° C. and slowly quenched into a 2N HCl solution (27.7 L). The quenched mixture was then stirred for 1 h at 40° C. Ammonium hydroxide concentrated (6.3 L) was added and the aqueous layer was discarded. i-PrOAc (18.5 L) and 5% dibasic sodium phosphate (18.5 L) were charged. The organic phase was then washed with saturated brine (18.5 L), dried over magnesium sulfate, filtered and evaporated to afford title compound 487 (4.63 g, 100%).

後処理

  1. customovernight
  2. customat 4° C.
  3. temperatureThe mixture was cooled to −5° C.
  4. additionborane-methyl sulfide complex (4.4 mL, 44.0 mmol) was added over 2 hours via syringe pump
  5. temperatureThe reaction mixture was then gradually warmed to 40° C. over 3 hours
  6. waitAfter aging 1.5 hours at 40° C.
  7. temperaturethe reaction mixture was cooled to 20-25° C.
  8. customslowly quenched into a 2N HCl solution (27.7 L)
  9. stirringThe quenched mixture was then stirred for 1 h at 40° C
  10. concentrationAmmonium hydroxide concentrated (6.3 L)
  11. additionwas added
  12. additioni-PrOAc (18.5 L) and 5% dibasic sodium phosphate (18.5 L) were charged
  13. washThe organic phase was then washed with saturated brine (18.5 L)
  14. dry with materialdried over magnesium sulfate
  15. filtrationfiltered
  16. customevaporated

出典と根拠

ORDレコード
ord-45f1c01556e54810a95dc253b0395dc2
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09193749B2

反応ノート

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