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(S)-tert-butyl 5,6-di(nitrooxy)hexanoate → (S)-5,6-di(nitrooxy)hexanoic acid

HRID 1675998
Notes
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Reaction equation

HRID 1675998 reaction equation
[N+:1]([O:4][C@H:5]([CH2:16][O:17][N+:18]([O-:20])=[O:19])[CH2:6][CH2:7][CH2:8][C:9]([O:11]C(C)(C)C)=[O:10])([O-:3])=[O:2]>C(Cl)Cl>[N+:1]([O:4][C@H:5]([CH2:16][O:17][N+:18]([O-:20])=[O:19])[CH2:6][CH2:7][CH2:8][C:9]([OH:11])=[O:10])([O-:3])=[O:2]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 59509520(S)-tert-butyl 5,6-di(nitrooxy)hexanoate

Product 1

HCID 29923588(S)-5,6-di(nitrooxy)hexanoic acid

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Conditions

Temperature
0 °C

Procedure

To a solution of (S)-tert-butyl 5,6-di(nitrooxy)hexanoate (12.41 g, 42.155 mmol) in DCM (47 mL) cooled to 0° C. under N2, boron trifluoride diethyl ether complex (5.82 mL, 46.37 mmol) was added. The reaction mixture was stirred at 0° C. for 10 minutes and at rt for 3 hrs. The solution was washed with brine, the organic layer was separated, dried over sodium sulfate and concentrated under reduced pressure. The crude brown oil was used in the next step without further purification.

Workup

  1. additionboron trifluoride diethyl ether complex (5.82 mL, 46.37 mmol) was added
  2. washThe solution was washed with brine
  3. customthe organic layer was separated
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe crude brown oil was used in the next step without further purification

Sources & evidence

ORD record
ord-24534e9923e848248099591fd173c9c3
Source dataset
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08003811B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes