Formaldehyde → 2-Cyano-2-(4-chlorophenyl)propan-1-ol

HRID 616390

반응식

HRID 616390 반응식
[CH3:1][CH:2]([C:10]#[N:11])[C:3]1[CH:8]=[CH:7][C:6]([Cl:9])=[CH:5][CH:4]=1.N1C=CC=CC=1.[CH2:18]=[O:19].[OH-].C([N+](CC)(CC)CC)C1C=CC=CC=1>O>[C:10]([C:2]([C:3]1[CH:4]=[CH:5][C:6]([Cl:9])=[CH:7][CH:8]=1)([CH3:1])[CH2:18][OH:19])#[N:11]

참가 물질

6

반응물 4

HCID 712FormaldehydeHCID 1049PyridineHCID 74601Benzyltriethylammonium hydroxideHCID 1027622-(4-Chlorophenyl)propiononitrile

생성물 1

HCID 140328512-Cyano-2-(4-chlorophenyl)propan-1-ol

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To an ice cold stirred solution of α-methyl-4-chlorobenzyl cyanide* (50g., 0.3 mole) in 500 ml. of pyridine containing a suspension of paraformaldehyde (36g., 1.2 mole) is added 1 ml. of benzyl triethylammonium hydroxide. The mixture is stirred under nitrogen at room temperature for 72 hours. The reaction mixture is poured into water and extracted with ether. The combined ether extracts are washed with water, saturated sodium chloride solution and dried over magnesium sulfate. The solvent is evaporated to give a thick oil, 58.4g, which is identified by nmr.

후처리

  1. additionis added 1 ml
  2. extractionextracted with ether
  3. washThe combined ether extracts are washed with water, saturated sodium chloride solution
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent is evaporated
  6. customto give a thick oil, 58.4g, which

출처 및 근거

ORD 기록
ord-b2b3a889c82949b2b1df201782405516
출처 데이터셋
uspto-grants-1978_02
특허 번호
US04073921

연결된 노트

불러오는 중…