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Trichloroacetic Acid → 5-Methoxy-2,6-dimethylheptan-1-ol

HRID 1974191
ノート
印刷プレビュー

反応式

HRID 1974191 の反応式
C[O:2][CH:3](OC)[CH:4]([CH3:13])[CH2:5][CH2:6][CH:7]([O:11][CH3:12])[CH:8]([CH3:10])[CH3:9].ClC(Cl)(Cl)C(O)=O.[OH-].[Na+].[BH4-].[Na+]>CO.O.O1CCCC1>[OH:2][CH2:3][CH:4]([CH3:13])[CH2:5][CH2:6][CH:7]([O:11][CH3:12])[CH:8]([CH3:9])[CH3:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 6421Trichloroacetic AcidHCID 14798Sodium HydroxideHCID 4311764Sodium borohydrideHCID 213990641,1,5-Trimethoxy-2,6-dimethylheptane

生成物 1

HCID 213991185-Methoxy-2,6-dimethylheptan-1-ol

試薬・触媒・溶媒 3

HCID 887Methanol溶媒
HCID 962
Water
溶媒
HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of 10.9 g. of 1,1,5-trimethoxy-2,6-dimethylheptane in 200 ml. of tetrahydrofuran and 60 ml. of water is treated with 1 g. of trichloroacetic acid and then the mixture heated at 60° for 1 hour. After cooling, there is added 40 ml. of 2N sodium hydroxide in methanol followed by 2 g. of powdered sodium borohydride. The reaction mixture is stirred at room temperature for 3 hours and then concentrated and extracted with ether. The ethereal extracts are evaporated under reduced pressure to give crude 1-hydroxy-5-methoxy-2,6-dimethylheptane which can be purified by distillation.

後処理

  1. temperatureAfter cooling
  2. additionthere is added 40 ml
  3. concentrationconcentrated
  4. extractionextracted with ether
  5. customThe ethereal extracts are evaporated under reduced pressure

出典と根拠

ORDレコード
ord-bed239cd1d824a77b7440c6fc18c94d3
出典データセット
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04000174

反応ノート

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