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Potassium periodate → tert-butyl N-(2-oxoethyl)carbamate

HRID 50098
Notes
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Reaction equation

HRID 50098 reaction equation
[C:1]([NH:8][CH2:9][CH:10]([OH:13])CO)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].I([O-])(=O)(=O)=O.[K+]>O>[C:1]([NH:8][CH2:9][CH:10]=[O:13])([O:3][C:4]([CH3:5])([CH3:6])[CH3:7])=[O:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 516896Potassium periodateHCID 4206999tert-butyl N-(2,3-dihydroxypropyl)carbamate

Product 1

HCID 4247255tert-butyl N-(2-oxoethyl)carbamate

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

3-Bocamino-1,2-propanediol (144.7 g; 0.757 mol) was suspended in water (750 ml) and potassium periodate (191.5 g; 0.833 mol) was added. The mixture was stirred under nitrogen for 2.5 h and the precipitated potassium iodate was removed by filtration and washed once with water (100 ml). The aqueous phase was extracted with chloroform (6×400 ml). The chloroform extracts were dried and evaporated to dryness, in vacuo. Yield 102 g (93%) of an oil. The (bocamino)acetaldehyde was purified by kugelrohr distillation at 84° C. and 0.3 mmHg in two portions. The yield 79 g (77%) of a colorless oil.

Workup

  1. customthe precipitated potassium iodate was removed by filtration
  2. washwashed once with water (100 ml)
  3. extractionThe aqueous phase was extracted with chloroform (6×400 ml)
  4. dry with materialThe chloroform extracts were dried
  5. customevaporated to dryness, in vacuo
  6. distillationThe (bocamino)acetaldehyde was purified by kugelrohr distillation at 84° C.

Sources & evidence

ORD record
ord-f1b1fd289cf747e08cc586886c20c191
Source dataset
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06710163B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes