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Chemical Structure| 61882-39-1 Chemical Structure| 61882-39-1

Structure of 61882-39-1

Chemical Structure| 61882-39-1

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Product Details of [ 61882-39-1 ]

CAS No. :61882-39-1
Formula : C5H9ClO2
M.W : 136.58
SMILES Code : O=C(Cl)CCCOC
MDL No. :MFCD20484189

Safety of [ 61882-39-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314-H335
Precautionary Statements:P260-P264-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P403+P233-P405-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 61882-39-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 61882-39-1 ]

[ 61882-39-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 29006-02-8 ]
  • [ 61882-39-1 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In Petroleum ether; (2) Preparation of 4-methoxybutyryl chloride 27 g (0.23 moles) of <strong>[29006-02-8]4-methoxybutyric acid</strong> were suspended in 150 cc of petroleum ether. To the resulting mixture a solution of 25 cc of thionyl chloride in 50 cc of petroleum ether was slowly added. The resulting mixture was kept under stirring overnight at room temperature. The raw product thus obtained was used as such in the subsequent reaction.
With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; at 20℃; for 2h; Oxalyl chloride and (3.5 mL) and DMF (1 drop) was added to <strong>[29006-02-8]4-methoxy-butyric acid</strong> methylene chloride solution of (761mg) (3.5mL), and the reaction mixture was stirred for 2 hours at room temperature.The reaction mixture was concentrated under reduced pressure, the residue was dissolved in methylene chloride (1 mL), ice cold methylene chloride solution (9.0 mL) of the compound obtained in Reference Example 137 (1.0g) and triethylamine (1.28 mL) It was dropped under.After stirring for 1 hour the reaction mixture at room temperature, water and saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, the mixture was extracted twice with chloroform.The organic layer was dried over anhydrous sodium sulfate to afford filtration, the title compound by concentrating (1.7g).MS (ESI) M / Z; 318 [M Tasu H]Tasu
With thionyl chloride; In toluene; at 0 - 120℃; for 3h; To the stirred solution of <strong>[29006-02-8]4-methoxy-butyric acid</strong> (18.0 g, 0.15 mol) in toluene (100 mL) was added thionyl chloride (11.3 mL, 0.15 mol) at 0 C. After addition temperature of the reactionmixture was slowly raised to RT and then refluxed at 120 C for 3 h. The reaction was monitored by TLC and after completion of the reaction; solvent was distilled off to give 19.0 g crude; which was directly used for the next step without purification.
  • 2
  • [ 79-37-8 ]
  • [ 29006-02-8 ]
  • [ 61882-39-1 ]
YieldReaction ConditionsOperation in experiment
In toluene; at 0 - 20℃; 4-Methoxybutyric acid (10 g) in toluene (50 ml) was added dropwise to a stirred solution of oxalyl chloride (8 ml) in toluene (50 ml) at ice bath temperature. Upon complete addition, the reaction was allowed to warm to RT and stirred overnight. Reaction mixture was evaporated to dryness to give the product which was used immediately.
  • 3
  • [ 61882-39-1 ]
  • [ 57497-39-9 ]
  • C9H19NO3 [ No CAS ]
 

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