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Sodium Bicarbonate → HCID 86014564, compound

HRID 2277027
Notes
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Reaction equation

HRID 2277027 reaction equation
[OH:1][C:2]1[CH:7]=[C:6]([CH2:8][CH2:9][CH2:10][CH2:11][OH:12])[O:5][C:4](=[O:13])[C:3]=1[C:14](=[O:17])[CH2:15][CH3:16].[Na].C([O-])(O)=O.[Na+]>C(Cl)Cl.N1C=CC=CC=1>[OH:1][C:2]1[CH:7]=[C:6]([CH2:8][CH2:9][CH2:10][CH:11]=[O:12])[O:5][C:4](=[O:13])[C:3]=1[C:14](=[O:17])[CH2:15][CH3:16]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 516892Sodium BicarbonateHCID 5360545SodiumHCID 68030291HCID 68030291, compound

Product 1

HCID 86014564HCID 86014564, compound

Reagents, catalysts & solvents 2

HCID 1049PyridineSolventHCID 6344DichloromethaneSolvent

Conditions

Temperature
28 °C

Procedure

To 4-hydroxy-6-(4-hydroxybutyl)-3-propionyl-2H-pyran-2-one (XV; 1.47 g; 6.12 mmol) in 60 ml CH2Cl2 and 2.19 ml pyridine, was added sodium periodinate (6.13 g; 15.3 mmol; Aldrich). The reaction was stirred at 28° C. for 3 h, neutralized with saturated NaHCO3, extracted with 3×150 ml CH2Cl2, dried with brine and Na2SO4, and evaporated. The product was purified via silica flash chromatography (20% EtOAc in hexanes).

Workup

  1. extractionextracted with 3×150 ml CH2Cl2
  2. dry with materialdried with brine and Na2SO4
  3. customevaporated
  4. customThe product was purified via silica flash chromatography (20% EtOAc in hexanes)

Sources & evidence

ORD record
ord-f4926f6d344e43bcab4293bbf0db2af9
Source dataset
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09133155B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes