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3-Chloro-1-propanol → HCID 18755438, compound

HRID 1838729
Notes
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Reaction equation

HRID 1838729 reaction equation
Cl[CH2:2][C:3]1[CH:8]=[C:7]([F:9])[CH:6]=[CH:5][C:4]=1[O:10][CH3:11].[Cl:12][CH2:13][CH2:14][CH2:15][OH:16].[H-].[Na+]>CN(C)C=O>[Cl:12][CH2:13][CH2:14][CH2:15][O:16][CH2:2][C:3]1[CH:8]=[C:7]([F:9])[CH:6]=[CH:5][C:4]=1[O:10][CH3:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 123133-Chloro-1-propanolHCID 24758Sodium hydride2×HCID 3026862-(Chloromethyl)-4-fluoro-1-methoxybenzene

Product 1

HCID 18755438HCID 18755438, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

0.870 g (5.00 mmol) of 2-chloromethyl-4-fluoro-1-methoxy-benzene [B. Maziere, N. Dat-Xuong, Chim. Ther. (3), 1-9(1968)]and 0.83 ml of 3-chloro-1-propanol were dissolved in 4.8 ml of N,N-dimethylformamide. 0.267 g (6.23 mmol) of sodium hydride (55% dispersion in mineral oil) was added in small portions over 2 hours keeping the temperature at 10-15° C. After 1 hour stirring at room temperature, 0.032 g (0.75 mmol) of sodium hydride dispersion was added and the mixture stirred another 3 hours. Thereupon, the reaction mixture was poured into 50 ml of ice-water and extracted three times with 100 ml of ether. The combined ether phases were subsequently washed with water, dried over magnesium sulphate and evaporated on a rotary evaporator at a maximum 40° C. The residue (1.5 g) which was thereby obtained was chromatographed on silica gel with dichloromethane/hexane (1:1). There was thus obtained 0.928 g (3.99 mmol), 80%,2-(3-chloro-propoxymethyl)-4-fluoro-1-methoxy-benzene as a colorless oil: MS: 232, 234 (M)+.

Workup

  1. customat 10-15° C
  2. stirringthe mixture stirred another 3 hours
  3. extractionextracted three times with 100 ml of ether
  4. washThe combined ether phases were subsequently washed with water
  5. dry with materialdried over magnesium sulphate
  6. customevaporated on a rotary evaporator at a maximum 40° C

Sources & evidence

ORD record
ord-59ae38dde3c1427ca515a2835ac699f4
Source dataset
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06673931B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes