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Ethyl Acetate → HCID 10279786, compound

HRID 1781457
Notes
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Reaction equation

HRID 1781457 reaction equation
[CH:1]([C:4]1[CH:11]=[C:10]([CH:12]([CH3:14])[CH3:13])[CH:9]=[C:8]([CH:15]([CH3:17])[CH3:16])[C:5]=1[CH2:6]Br)([CH3:3])[CH3:2].[CH:18]([C:21]1[CH:33]=[CH:32][CH:31]=[C:30]([CH:34]([CH3:36])[CH3:35])[C:22]=1[O:23][S:24]([N:27]=C=O)(=[O:26])=[O:25])([CH3:20])[CH3:19].[NH4+].[Cl-].C[CH2:40][O:41]C(C)=O>C1COCC1>[CH3:2][CH:1]([C:4]1[CH:11]=[C:10]([CH:12]([CH3:14])[CH3:13])[CH:9]=[C:8]([CH:15]([CH3:17])[CH3:16])[C:5]=1[CH2:6][C:40]([C:33]1[C:21]([CH:18]([CH3:19])[CH3:20])=[C:22]([O:23][S:24](=[O:25])(=[O:26])[NH2:27])[C:30]([CH:34]([CH3:35])[CH3:36])=[CH:31][CH:32]=1)=[O:41])[CH3:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 8857Ethyl AcetateHCID 25517Ammonium ChlorideHCID 10590086HCID 10590086, compoundHCID 106367162,6-Diisopropylphenoxysulfonyl isocyanate

Product 1

HCID 10279786HCID 10279786, compoundYield 67%

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent
2×

Procedure

A solution of 2,4,6-triisopropylbenzyl bromide (12 g, 40.4 retool) in dry THF (160 nIL) was added to a suspension of Mg powder (1.96 g, 80.8 retool) (4 hours) in THF (20 mL) heated under reflux. 2,6-Diisopropylphenoxysulfonyl isocyanate (ROSO2NCO) (see Phos. and Sulf., 19:167 (1984) for preparation) (11.45 g, 40.4 mmol) was added neat, and after the addition was completed, the reflux was continued for another 2 hours. The reaction was stirred at room temperature for 16 hours. Saturated NH4Cl and EtOAc were added. The EtOAc layer was separated, dried over MgSO4, filtered, and evaporated to dryness. After purification by column chromatography (4:1 hexane:EtOAc), the compound was isolated as white solid (13.5 g, 67%), mp .178°-180° C.

Workup

  1. temperatureheated
  2. temperatureunder reflux
  3. additionafter the addition
  4. customThe EtOAc layer was separated
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated to dryness
  8. customAfter purification by column chromatography (4:1 hexane:EtOAc)

Sources & evidence

ORD record
ord-59aa947432e84f2dacbc8cc686c3b4b5
Source dataset
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05633287

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes