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3-Chloro-1-propanol → Butanoic acid, 3-oxo-, 3-chloropropyl ester

HRID 330229
Notes
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Reaction equation

HRID 330229 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][OH:5].[CH2:6]=[C:7]1[O:11][C:9](=[O:10])[CH2:8]1>C(N(CC)CC)C>[C:9]([O:5][CH2:4][CH2:3][CH2:2][Cl:1])(=[O:10])[CH2:8][C:7]([CH3:6])=[O:11]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 123133-Chloro-1-propanolHCID 12661Diketene

Product 1

HCID 10511540Butanoic acid, 3-oxo-, 3-chloropropyl esterYield 82%

Reagents, catalysts & solvents 1

HCID 8471TriethylamineSolvent

Conditions

Temperature
65 °C

Procedure

3-Chloropropanol (47.3 g, 0.50 mole) and a catalytic amount of triethylamine at 65° C. were treated dropwise with 42 g (0.50 mole) of diketene. After the addition was complete, the reaction was stirred at 65° C. for an additional hour. Distillation of the residue furnished 72.9 g (82%) of product as a clear liquid, b.p. 78°-85° C. at 150 mm. Additional Formula II intermediates can be prepared by modifications of the above examples which would be understood by one skilled in the art of organic chemical synthesis.

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

  1. additionAfter the addition
  2. distillationDistillation of the residue

Sources & evidence

ORD record
ord-c45cc3c97de04b46b2f3d62d1f2167c3
Source dataset
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04895846

Reaction notes

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