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Water → (S)-(+)-1-Acetoxy-3-bromo-2-methyl-propane

HRID 219705
Notes
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Reaction equation

HRID 219705 reaction equation
[Br:1][CH2:2][C@@H:3]([CH3:6])[CH2:4][OH:5].[C:7](OC(=O)C)(=[O:9])[CH3:8].O.C(OCC)(=O)C>N1C=CC=CC=1>[C:7]([O:5][CH2:4][C@H:3]([CH3:6])[CH2:2][Br:1])(=[O:9])[CH3:8]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 7918Acetic AnhydrideHCID 8857Ethyl AcetateHCID 10986449(S)-(+)-3-Bromo-2-methyl-1-propanol

Product 1

HCID 10465240(S)-(+)-1-Acetoxy-3-bromo-2-methyl-propaneYield 68.3%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Conditions

Temperature
70 °C

Procedure

5 g of (S)-(+)-3-bromo-2-methyl-1-propanol (32.6 mmol) were stirred in 5 ml of pyridine at room temperature. 3.67 g of acetic anhydride (35.9 mmol) were added and the reaction mixture was stirred for 3 h at 70° C. Stirring was continued for 16 h at room temperature. 30 ml of water and 40 ml of ethyl acetate were added. The organic layer was separated and washed with a further portion of water, then dried over magnesium sulfate, filtered, and evaporated under reduced pressure, whereby 4.34 g of the title compound were obtained.

Workup

  1. stirringStirring
  2. waitwas continued for 16 h at room temperature
  3. customThe organic layer was separated
  4. washwashed with a further portion of water
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-11aa72148de94870880eb1a437376a8e
Source dataset
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08202868B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes