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Chemical Structure| 108221-67-6 Chemical Structure| 108221-67-6

Structure of 108221-67-6

Chemical Structure| 108221-67-6

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Product Details of [ 108221-67-6 ]

CAS No. :108221-67-6
Formula : C5H8BrFO2
M.W : 199.02
SMILES Code : CC(F)(Br)C(OCC)=O
MDL No. :MFCD33394997

Safety of [ 108221-67-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H315-H319-H335
Precautionary Statements:P210-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501
Class:3
UN#:1993
Packing Group:

Application In Synthesis of [ 108221-67-6 ]

* 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 [ 108221-67-6 ]

[ 108221-67-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 349-43-9 ]
  • [ 108221-67-6 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; dibenzoyl peroxide;bromine; In tetrachloromethane; for 1h;Reflux; Example 2To 416 mL of carbon tetrachloride, 100 g (833 mmol, 1.00 eq) of <strong>[349-43-9]ethyl 2-fluoropropionate</strong> of the following formula, 163 g (916 mmol, 1.10 eq) of N-bromosuccinimide (NBS), 13.5 g (water content: 25percent, 41.8 mmol, 0.05 eq) of benzoyl peroxide (BPO) and 13.3 g (83.2 mmol, 0.10 eq) of bromine (Br2) were added. The resulting reaction liquid was stirred for 1 hour under reflux conditions. The rate of conversion to ethyl 2-bromo-2-fluoropropionate of the following formula in the reaction terminated liquid was determined by gas chromatography to be 74percent.
In a 250 ml Erlenmeyer flask with a condenser, 12.0 g (0.1 mol) of <strong>[349-43-9]ethyl 2-fluoropropionate</strong> and 180 g of 1,2-difluorotetrachloroethane were added.24.0 g (0.15 mol) of bromine, 22.5 g (0.15 mol) of sodium dihydrogen phosphate, and 0.2 g of t-butyl peroxide were stirred and irradiated with an ultraviolet lamp having a wavelength of 254 nm.The reaction was carried out by heating to 90 ° C in an oil bath.After 12 h, 0.2 g of t-butyl peroxide was added and the reaction was carried out for 24 h. The conversion of <strong>[349-43-9]ethyl 2-fluoropropionate</strong> was 88.3percent.The selectivity to ethyl 2-fluoro-2-bromopropionate was 87.2percent.
With sulfuryl dichloride; 2,2'-azobis(isobutyronitrile); bromine; In tetrachloromethane; at 70℃; for 10h; Add 12.0 g (0.1 mol) to a 250 ml four-necked flask with a condenser<strong>[349-43-9]Ethyl 2-fluoropropionate</strong>,240g of carbon tetrachloride,24.0 g (0.15 mol) of bromine,20.2 g (0.15 mol) of sulfuryl chloride,0.6g azoisobutyronitrile,StirThe reaction was carried out by heating to 70 °C.After 10 h, the conversion of m<strong>[349-43-9]ethyl 2-fluoropropionate</strong> was 98.2percent.The selectivity to ethyl 2-fluoro-2-bromopropionate was 88.4percent.
 

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