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Hydrochloric Acid → p-(Octylthiomethyl)benzyl chloride

HRID 8423
Notes
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Reaction equation

HRID 8423 reaction equation
CC(C)([O-])C.[Na+].[CH2:7]([SH:15])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].[C:16]1([CH2:24]Cl)[CH:21]=[CH:20][C:19]([CH2:22][Cl:23])=[CH:18][CH:17]=1.Cl>CO>[CH2:7]([S:15][CH2:24][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][Cl:23])=[CH:18][CH:17]=1)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 81441-OctanethiolHCID 12171alpha,alpha'-Dichloro-p-xyleneHCID 23676156Sodium t-butoxide

Product 1

HCID 10613099p-(Octylthiomethyl)benzyl chloride

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Procedure

1.83 g (19 mmol) of sodium t-butoxide and 2.78 g (19 mmol) of octanethiol were stirred into 40 g of methanol at room temperature. After 30 minutes, the clear solution was added in one portion to 3.33 g (19 mmol) of p-xylylene dichloride in 100 g of methanol. After one hour, the mixture was neutralized using 1N hydrochloric acid, and all the volatile components were removed under reduced pressure. The crude product was taken up in 250 ml of chloroform and washed twice with 100 ml of water each time, dried and evaporated under reduced pressure. 5.29 g, which, according to 1H-NMR-spectroscopy, consisted of 50% of product, 25% of starting material and 25% of p-bis(octylthiomethyl)benzene.

Workup

  1. waitAfter one hour
  2. customall the volatile components were removed under reduced pressure
  3. washwashed twice with 100 ml of water each time
  4. customdried
  5. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-1dafe2e64013446290804c2d6d9417a2
Source dataset
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07087787B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes