HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Sodium periodate → Ethyl 2-(4-bromo-2-chlorobenzyl)-4-oxobutanoate

HRID 1013804
Notes
Print preview

Reaction equation

HRID 1013804 reaction equation
I([O-])(=O)(=O)=[O:2].[Na+].[Br:7][C:8]1[CH:23]=[CH:22][C:11]([CH2:12][CH:13]([CH2:19][CH:20]=C)[C:14]([O:16][CH2:17][CH3:18])=[O:15])=[C:10]([Cl:24])[CH:9]=1>C1COCC1.O.O=[Os](=O)(=O)=O>[Br:7][C:8]1[CH:23]=[CH:22][C:11]([CH2:12][CH:13]([CH2:19][CH:20]=[O:2])[C:14]([O:16][CH2:17][CH3:18])=[O:15])=[C:10]([Cl:24])[CH:9]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 2

HCID 23667635Sodium periodateHCID 67316264Ethyl 2-(4-bromo-2-chlorobenzyl)pent-4-enoate

Product 1

HCID 86629116Ethyl 2-(4-bromo-2-chlorobenzyl)-4-oxobutanoateYield 75.7%

Reagents, catalysts & solvents 3

HCID 30318Osmium TetroxideCatalystHCID 962WaterSolvent
HCID 8028
Tetrahydrofuran
Solvent

Procedure

Add sodium periodate (41 g, 190 mmol) into a solution of ethyl 2-(4-bromo-2-chlorobenzyl)pent-4-enoate (21 g, 63 mmol), 2.5 wt % OsO4 (64 g, 6.3 mmol) in THF (400 mL) and water (160 mL) and stir for 2 hours. Extract the reaction mixture with ethyl acetate, wash the organic layer with sodium thiosulfate solution and brine. Dry over sodium sulfate, filter and concentrate. Purify the residue with silica gel column to afford the title compound (15.9 g, 75%) as colorless oil: 1H NMR (CDCl3) 9.73 (s, 1H), 7.53 (d, J=2.0 Hz, 1H), 7.32 (dd, J=8.20, 2.0 Hz, 1H), 7.08 (d, J=8.2 Hz, 1H), 4.05-4.15 (m, 2H), 3.20-3.28 (m, 1H), 3.07-3.15 (m, 1H), 2.84-2.92 (m, 2H), 2.53-2.61 (m, 1H), 1.51-1.21 (m, 3H).

Workup

  1. extractionExtract the reaction mixture with ethyl acetate
  2. washwash the organic layer with sodium thiosulfate solution and brine
  3. dry with materialDry over sodium sulfate
  4. filtrationfilter
  5. concentrationconcentrate
  6. customPurify the residue with silica gel column

Sources & evidence

ORD record
ord-0d43f0541051410c8b6fcf2aa5d5aa48
Source dataset
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07981918B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes