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1,4-Dioxane → 1-(Methoxymethyl)-3-oxocyclobutane-1-carbonitrile

HRID 1692921
Notes
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Reaction equation

HRID 1692921 reaction equation
[O:1]1CCOCC1.[CH3:7][O:8][CH2:9][C:10]1([C:15]#[N:16])[CH2:13][C:12](=C)[CH2:11]1.I([O-])(=O)(=O)=O.[Na+]>O.[Os](=O)(=O)(=O)=O>[CH3:7][O:8][CH2:9][C:10]1([C:15]#[N:16])[CH2:13][C:12](=[O:1])[CH2:11]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 312751,4-DioxaneHCID 23667635Sodium periodateHCID 668243071-(Methoxymethyl)-3-methylidenecyclobutane-1-carbonitrile

Product 1

HCID 668243301-(Methoxymethyl)-3-oxocyclobutane-1-carbonitrile

Reagents, catalysts & solvents 2

HCID 30318Osmium TetroxideCatalyst
HCID 962
Water
Solvent
2×

Procedure

A mixture of water (2 mL, 0.1 mol) and 1,4-dioxane (7 mL, 0.08 mol), 1-(methoxymethyl)-3-methylenecyclobutanecarbonitrile (0.294 g, 0.00214 mol), and 0.2 M of osmium tetraoxide in water (0.04 mL) was stirred for 5 min, during which time the mixture became brown. While the temperature was maintained at room temperature, sodium periodate (0.963 g, 0.00450 mol) was added in portions over a period of 30 min. The mixture was stirred overnight. The mixture was extracted with EtOAc and the combined organic layers were dried over MgSO4. After removal of the solvents, the crude product was used directly in next step (298 mg, 99.92%). 1H NMR (400 MHz, CDCl3): 3.70 (2H, s), 3.68 (3H, s), 3.58 (2H, m), 3.38 (2H, m) ppm.

Workup

  1. stirringThe mixture was stirred overnight
  2. extractionThe mixture was extracted with EtOAc
  3. dry with materialthe combined organic layers were dried over MgSO4
  4. customAfter removal of the solvents

Sources & evidence

ORD record
ord-8ea74a97d5ac4d97a808eaf3bc540c3b
Source dataset
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08158616B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes