Triethylamine → 1-Allyloxy-4-chloromethyl-benzene

HRID 1392222Notes

Reaction equation

HRID 1392222 reaction equation
CS([Cl:5])(=O)=O.[CH2:6]([O:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16]O)=[CH:12][CH:11]=1)[CH:7]=[CH2:8].C(N(CC)CC)C>ClCCl>[CH2:6]([O:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][Cl:5])=[CH:12][CH:11]=1)[CH:7]=[CH2:8]

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 11744970(4-(Prop-2-en-1-yloxy)phenyl)methanol

Product 1

HCID 123479361-Allyloxy-4-chloromethyl-benzene

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

7.67 g (67.0 mmol) methanesulfonyl chloride were given at 0° C. to a solution of 10.0 g (60.9 mmol) (4-allyloxy-phenyl)-methanol and 9.34 ml (67.0 mmol) triethylamine in 35 ml dichloromethane and stirred at r.t. overnight. The mixture was poured in ice water, extracted with dichloromethane and the organic phase dried over Na2SO4. After removal of solvents the residue was purified by chromatography on silica gel (ethyl acetate/n-heptane 1:5) to yield 3.12 g (28%) pale yellow oil.

Workup

  1. extractionextracted with dichloromethane
  2. dry with materialthe organic phase dried over Na2SO4
  3. customAfter removal of solvents the residue
  4. customwas purified by chromatography on silica gel (ethyl acetate/n-heptane 1:5)
  5. customto yield 3.12 g (28%)

Sources & evidence

ORD record
ord-a8c6c91558bc47f39ba9d1d18f9b216e
Source dataset
uspto-grants-2008_03
Patent number
US07342030B2

Reaction notes

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