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Tributyltin Chloride → 2-((Tert-butyldimethylsilyloxy)methyl)-5-(tributylstannyl)thiazole

HRID 589190
Notes
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Reaction equation

HRID 589190 reaction equation
[Si:1]([O:8][CH2:9][C:10]1[S:11][CH:12]=[CH:13][N:14]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[Li]C(C)(C)C.[Sn:20](Cl)([CH2:29][CH2:30][CH2:31][CH3:32])([CH2:25][CH2:26][CH2:27][CH3:28])[CH2:21][CH2:22][CH2:23][CH3:24].[NH4+].[Cl-]>C1COCC1>[Si:1]([O:8][CH2:9][C:10]1[S:11][C:12]([Sn:20]([CH2:25][CH2:26][CH2:27][CH3:28])([CH2:29][CH2:30][CH2:31][CH3:32])[CH2:21][CH2:22][CH2:23][CH3:24])=[CH:13][N:14]=1)([C:4]([CH3:7])([CH3:5])[CH3:6])([CH3:2])[CH3:3]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 15096Tributyltin ChlorideHCID 25517Ammonium ChlorideHCID 214805922-((Tert-butyldimethylsilyloxy)methyl)thiazoleHCID 178418306HCID 178418306, compound

Product 1

HCID 672943522-((Tert-butyldimethylsilyloxy)methyl)-5-(tributylstannyl)thiazoleYield 77.7%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-78 °C

Procedure

2-((tert-butyldimethylsilyloxy)methyl)thiazole (8.0 g, 35 mmol) was dissolved in dry THF (350 mL) and the solution was cooled to −78° C. To this solution, t-BuLi (1.7 M, 25 mL, 42 mmol) was added dropwise. The reaction was warmed to −40° C. and stirred for 2 hours. Then, Bu3SnCl (14.6 g, 45 mmol) was added and the resulting mixture was allowed to warm to room temperature slowly and stirred for another 30 min. NH4Cl (aq.) was added to quench the reaction and extracted with EtOAc. The organics was dried and concentrated. The residue was purified with column (silica gel, 0˜30 EtOAc/hexane) to give the product 2-((tert-butyldimethylsilyloxy)methyl)-5-(tributylstannyl)thiazole (14.1 g)

Workup

  1. temperatureThe reaction was warmed to −40° C.
  2. temperatureto warm to room temperature slowly
  3. stirringstirred for another 30 min
  4. customto quench
  5. customthe reaction
  6. extractionextracted with EtOAc
  7. customThe organics was dried
  8. concentrationconcentrated
  9. customThe residue was purified with column (silica gel, 0˜30 EtOAc/hexane)

Sources & evidence

ORD record
ord-481e3b87cacc44ddbbcc93050697583b
Source dataset
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09227971B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes