Benzyl Alcohol → Benzyl 2-bromopropanoate

HRID 963122

反応式

HRID 963122 の反応式
[Br:1][CH:2]([CH3:6])[C:3]([OH:5])=[O:4].[CH2:7](O)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.C1(N=C=NC2CCCCC2)CCCCC1>C(Cl)Cl.CN(C)C1C=CN=CC=1>[CH2:7]([O:4][C:3](=[O:5])[CH:2]([Br:1])[CH3:6])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

参加物

6

反応物 3

HCID 244Benzyl AlcoholHCID 10868DicyclohexylcarbodiimideHCID 117292-Bromopropionic acid

生成物 1

HCID 298874Benzyl 2-bromopropanoate

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane溶媒2 回

実験手順

20.0 g (0.13 moles) of 2-bromopropionic acid were stirred with 14.1 g (0.13 moles) of benzyl alcohol in dry methylene chloride at 5°-10° C., before 0.16 g (1.3e-3 moles) of 4-dimethylaminopyridine (DMAP) were added. The temperature was raised to ~15° C. before a solution of dicyclohexylcarbodiimide (DCC) (26.7 g, 0.13 moles) in dry methylene chloride was added dropwise. The solution was added at a rate as to not increase the reaction temperature above 35° C. After the imide addition was complete, the reaction proceeded at 25° C. for several hours or until infrared spectroscopy analysis indicated the absence of a carboxylic acid stretch at 1730 cm-1. Upon completion, the reaction mixture was filtered under vacuum to remove the dicyclohexyl urea (DCU) byproduct and the filtrate was extracted once with water, once with 5% acetic acid solution (to remove DMAP) and again with water. The organic layer was dried over anhydrous magnesium sulfate before being filtered and concentrated under reduced pressure. Yield was 25 g (72%) of a mixture of Benzyl-2-bromopropionate and Benzyl-2-chloropropionate.

後処理

  1. additionwere added
  2. additionwas added dropwise
  3. additionThe solution was added at a rate as to not
  4. temperatureincrease the reaction temperature above 35° C
  5. waitthe reaction proceeded at 25° C. for several hours
  6. filtrationUpon completion, the reaction mixture was filtered under vacuum
  7. customto remove the dicyclohexyl urea (DCU) byproduct
  8. extractionthe filtrate was extracted once with water, once with 5% acetic acid solution (to remove DMAP) and again with water
  9. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  10. filtrationbefore being filtered
  11. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-8f73987ecd814d8dba23b64f6f07b918
出典データセット
uspto-grants-1998_06
特許番号
US05762947

関連ノート

読み込み中…