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Thionyl Chloride → 1-(Chloromethyl)-4-fluoro-2-methylbenzene

HRID 749466
Notes
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Reaction equation

HRID 749466 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8]O)=[C:4]([CH3:10])[CH:3]=1.O=S(Cl)[Cl:13]>C(Cl)Cl>[Cl:13][CH2:8][C:5]1[CH:6]=[CH:7][C:2]([F:1])=[CH:3][C:4]=1[CH3:10]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24386Thionyl ChlorideHCID 3872017(4-Fluoro-2-methylphenyl)methanol

Product 1

HCID 205118161-(Chloromethyl)-4-fluoro-2-methylbenzeneYield 100%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Conditions

Temperature
0 °C

Procedure

(4-Fluoro-2-methylphenyl)methanol (11.5 g, 82 mmol) was dissolved in CH2Cl2 (100 mL). The mixture was cooled to 0° C. before adding SOCl2 (10.7 g, 90 mmol), then stirred for 30 min at 0° C. and then at room temperature for 1.5 h. The solvent and excess of SOCl2 were removed by evaporation followed by the addition of CH2Cl2. The solvent and remaining traces of SOCl2 were evaporated once more. There was obtained 13.0 g (100%) of 1-(chloromethyl)-4-fluoro-2-methylbenzene as an oil. 1H NMR (300 MHz, CDCl3): 2.4 (s, 3H), 4.6 (s, 2H), 6.8-7.0 (m, 2H), 7.3 (m, 1H).

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

  1. waitat room temperature for 1.5 h
  2. customThe solvent and excess of SOCl2 were removed by evaporation
  3. additionfollowed by the addition of CH2Cl2
  4. customwere evaporated once more

Sources & evidence

ORD record
ord-e4780ea8b04548c3aacbdfe22a6d5b38
Source dataset
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07402581B2

Reaction notes

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