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Potassium Carbonate → 6-(4-Bromobenzyl)-2-oxa-6-aza-spiro[3.3]heptane

HRID 1505905
Notes
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Reaction equation

HRID 1505905 reaction equation
[CH2:1]1[C:4]2([CH2:7][NH:6][CH2:5]2)[CH2:3][O:2]1.[Br:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13]Br)=[CH:11][CH:10]=1.C(=O)([O-])[O-].[K+].[K+]>C1COCC1.[I-].[Na+]>[Br:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13][N:6]2[CH2:7][C:4]3([CH2:3][O:2][CH2:1]3)[CH2:5]2)=[CH:11][CH:10]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 11430Potassium CarbonateHCID 685274-Bromobenzyl bromideHCID 231118872-Oxa-6-azaspiro[3.3]heptane

Product 1

HCID 582664706-(4-Bromobenzyl)-2-oxa-6-aza-spiro[3.3]heptaneYield 68%

Reagents, catalysts & solvents 2

HCID 5238Sodium IodideCatalyst
HCID 8028
Tetrahydrofuran
Solvent

Procedure

A mixture of 2-oxa-6-aza-spiro[3.3]heptane (˜3.72 mmol), 4-bromobenzyl bromide (0.39 g, 1.54 mmol), potassium carbonate (0.64, 4.63 mmol) and sodium iodide (11 mg, 0.08 mmol) in THF (10 mL) was stirred at ambient temperature for 16 h. The solid was removed by filtration, washed with THF and the combined filtrate was evaporated. The resultant residue was purified by flash chromatography (silica, 12 g column, ISCO, 0-100% ethyl acetate in pentane then 10% methanol in DCM) to afford the title compound (0.28 g, 68%) as a viscous oil which crystallised on standing to a pale yellow solid. 1H NMR (CDCl3, 300 MHz): 7.46-7.40 (m, 2H), 7.15-7.09 (m, 2H), 4.73 (s, 4H), 3.48 (s, 2H), 3.35 (s, 4H).

Workup

  1. customThe solid was removed by filtration
  2. washwashed with THF
  3. customthe combined filtrate was evaporated
  4. customThe resultant residue was purified by flash chromatography (silica, 12 g column, ISCO, 0-100% ethyl acetate in pentane

Sources & evidence

ORD record
ord-d658c9ecb6f9490683db68a8587e1517
Source dataset
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09216980B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes