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1-Butanol → Butyl 4-(tert-butylperoxy)-4-methylpentan-2-yl carbonate

HRID 1856308
Notes
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Reaction equation

HRID 1856308 reaction equation
C([OH:5])CCC.N1C=[CH:10][CH:9]=[CH:8][CH:7]=1.Cl[C:13]([O:15][CH:16]([CH3:27])[CH2:17][C:18]([CH3:26])([O:20][O:21][C:22]([CH3:25])([CH3:24])[CH3:23])[CH3:19])=[O:14]>C(OCC)C>[C:13](=[O:5])([O:14][CH2:7][CH2:8][CH2:9][CH3:10])[O:15][CH:16]([CH3:27])[CH2:17][C:18]([CH3:26])([O:20][O:21][C:22]([CH3:25])([CH3:24])[CH3:23])[CH3:19]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 2631-ButanolHCID 1049PyridineHCID 19612317HCID 19612317, compound

Product 1

HCID 23346606Butyl 4-(tert-butylperoxy)-4-methylpentan-2-yl carbonate

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

To a solution of 8.1 g. (0.11 mole) of n-butyl alcohol and 7.9 g. (0.1 mole) of pyridine in diethyl ether cooled to 10°±1° C. was added a solution of 27.0 g. (0.1 mole) 1,3-dimethyl-3-(t-butylperoxy)butyl chloroformate. The reaction temperature was controlled at 15°±1° C. during the addition.

Workup

  1. additionwas added a solution of 27.0 g
  2. additionThe reaction temperature was controlled at 15°±1° C. during the addition

Sources & evidence

ORD record
ord-8346542ffcc3491888c5efe5fbc8cd23
Source dataset
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04218548

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes