Home Cart Sign in  
Chemical Structure| 22094-18-4 Chemical Structure| 22094-18-4
Chemical Structure| 22094-18-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Synonyms: 1,3-Dibromoacetone Dimethyl Acetal

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of 1,3-Dibromo-2,2-dimethoxypropane

CAS No. :22094-18-4
Formula : C5H10Br2O2
M.W : 261.94
SMILES Code : C(C(CBr)(OC)OC)Br
Synonyms :
1,3-Dibromoacetone Dimethyl Acetal
MDL No. :MFCD00051792
InChI Key :CPAHOXOBYHMHDT-UHFFFAOYSA-N
Pubchem ID :2734196

Safety of 1,3-Dibromo-2,2-dimethoxypropane

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of 1,3-Dibromo-2,2-dimethoxypropane

* 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.

  • Upstream synthesis route of [ 22094-18-4 ]
  • Downstream synthetic route of [ 22094-18-4 ]

[ 22094-18-4 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 67-56-1 ]
  • [ 67-64-1 ]
  • [ 22094-18-4 ]
YieldReaction ConditionsOperation in experiment
60% at 0 - 20℃; for 15 h; To a stirring solutionof compound 29.1(157g, 2.7 mol) in CH30H (1.6 L) at 0°Cwas added Br2 (950 g, 5.9 moL) dropwise, and the reactionwas stirred with warming tort for 15 hr. The precipitate was collected by filtration and was washed with cold methanol to yield5 compound29.2 (450 g, 60percent) as a white solid.
32% at 0 - 25℃; for 25 h; To a solution of acetone (12.6 ml) in methanol (150 ml), bromine (20 ml) was added dropwise over the time of 1 h. Initially the reaction was slightly exothermic so an ice bath was applied. Upon completion of addition, the ice bath was removed and the resulting deep red reaction was stirred at 25° C. for 24 h. After such time, the reaction was cooled in an ice/acetone bath and stirred for 1 h. Filtration of the precipitate and wash with cold methanol afforded 1,3-dibromo-2,2-dimethoxy-propane (14.72 g, 32percent) as a white solid: 1H NMR (300 MHz, CDCl3) δ ppm 3.30 (s, 6 H, 2.x.OCH3), 3.59 (s, 4 H, 2.x.BrCH2).
References: [1] Patent: WO2014/165075, 2014, A1, . Location in patent: Page/Page column 86; 87.
[2] Patent: US2008/21032, 2008, A1, . Location in patent: Page/Page column 83.
[3] Chemistry - A European Journal, 2011, vol. 17, # 2, p. 468 - 480.
[4] Patent: US2009/298894, 2009, A1, . Location in patent: Page/Page column 44.
[5] Patent: WO2016/44770, 2016, A1, . Location in patent: Page/Page column 752.
  • 2
  • [ 67-56-1 ]
  • [ 26562-24-3 ]
  • [ 22094-18-4 ]
  • [ 77416-08-1 ]
References: [1] Journal of the American Chemical Society, 1974, vol. 96, p. 4597 - 4603.
  • 3
  • [ 67-56-1 ]
  • [ 816-39-7 ]
  • [ 22094-18-4 ]
References: [1] Chemische Berichte, 1935, vol. 68, p. 1866 Anm.4.
  • 4
  • [ 67-56-1 ]
  • [ 77-76-9 ]
  • [ 22094-18-4 ]
  • [ 126-38-5 ]
References: [1] Synthetic Communications, 1980, vol. 10, # 11, p. 821 - 826.
  • 5
  • [ 67-56-1 ]
  • [ 67-64-1 ]
  • [ 22094-18-4 ]
  • [ 867-54-9 ]
  • [ 816-39-7 ]
  • [ 77416-08-1 ]
  • [ 77416-09-2 ]
References: [1] Journal of Organic Chemistry, 1981, vol. 46, # 12, p. 2532 - 2538.
 

Historical Records

Technical Information

Categories