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18-Crown-6 → 4,4,4-Trimethoxybutyl para-toluenethiosulphonate

HRID 567891
Notes
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Reaction equation

HRID 567891 reaction equation
[K+].[C:2]1([CH3:12])[CH:7]=[CH:6][C:5]([S:8](=[S:11])([O-:10])=[O:9])=[CH:4][CH:3]=1.[CH3:13][O:14][C:15]([O:22][CH3:23])([O:20][CH3:21])[CH2:16][CH2:17][CH2:18]Br.C1OCCOCCOCCOCCOCCOC1.C(=O)(O)[O-].[Na+]>O1CCCC1>[C:2]1([CH3:12])[CH:3]=[CH:4][C:5]([S:8](=[S:11])([O:10][CH2:18][CH2:17][CH2:16][C:15]([O:22][CH3:23])([O:20][CH3:21])[O:14][CH3:13])=[O:9])=[CH:6][CH:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 2855718-Crown-6HCID 516892Sodium BicarbonateHCID 5187924Trimethyl 4-bromoorthobutyrateHCID 23662126Benzenesulfonothioic acid, 4-methyl-, potassium salt (1:1)

Product 1

HCID 537006924,4,4-Trimethoxybutyl para-toluenethiosulphonateYield 89.3%

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent

Procedure

A suspension of para-toluenethiosulphonic acid potassium salt (8.77 g), trimethyl 4-bromoorthobutyrate (8.00 g) and 18-crown-6 (10.24 g) in anhydrous tetrahydrofuran (60 ml) was ultrasonicated for 5 minutes then stirred at room temperature for 3 days. The mixture was poured into saturated aqueous sodium bicarbonate solution (200 ml) and extracted with ether (2×200 ml). The organic extracts were dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to give the subtitle compound (10.52 g) as an oil.

Workup

  1. customwas ultrasonicated for 5 minutes
  2. extractionextracted with ether (2×200 ml)
  3. dry with materialThe organic extracts were dried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-52b6b5407fcf41488f088a0b8f5f0e28
Source dataset
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06180635B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes