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Benzenemethanethiol, alpha,alpha-diphenyl- → HCID 68599758, compound

HRID 2246074
Notes
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Reaction equation

HRID 2246074 reaction equation
[C:1]([C:3]1[S:7][CH:6]=[N:5][C:4]=1[CH2:8][OH:9])#[CH:2].[C:10]1([C:16]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[SH:17])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.CC(C)([O-])C.[K+]>C1COCC1.[Cl-].[Na+].O>[OH:9][CH2:8][C:4]1[N:5]=[CH:6][S:7][C:3]=1/[CH:1]=[CH:2]\[S:17][C:16]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)([C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1)[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 77281Benzenemethanethiol, alpha,alpha-diphenyl-HCID 23665647Potassium tert-butoxideHCID 45121755HCID 45121755, compound

Product 1

HCID 68599758HCID 68599758, compound

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolvent
HCID 57417360
Sodium chloride; water
Solvent

Procedure

A solution of 2.73 g of 5-ethynyl-4-hydroxymethylthiazole in 65 ml of THF was cooled in ice under an argon atmosphere, and 6.5 g of triphenylmethane thiol and 440 mg of potassium-t-butoxide were added to the cooled solution. The mixture was stirred at room temperature for 2 hr. Brine was added to the reaction solution, and the mixture was extracted twice with ethyl acetate. The organic layers were combined, were washed with brine, were then dried over anhydrous magnesium sulfate, were filtered, and were concentrated under the reduced pressure. Ethyl acetate (10 ml) and 10 ml of hexane were added to the residue, and the resultant precipitate was collected by filtration to give 7.26 of the title compound.

Workup

  1. extractionthe mixture was extracted twice with ethyl acetate
  2. washwere washed with brine
  3. dry with materialwere then dried over anhydrous magnesium sulfate
  4. filtrationwere filtered
  5. concentrationwere concentrated under the reduced pressure
  6. additionEthyl acetate (10 ml) and 10 ml of hexane were added to the residue
  7. filtrationthe resultant precipitate was collected by filtration

Sources & evidence

ORD record
ord-b0068b566c8b4e40aa49123868046e11
Source dataset
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07687490B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes