Home Cart Sign in  
Chemical Structure| 172103-12-7 Chemical Structure| 172103-12-7

Structure of 172103-12-7

Chemical Structure| 172103-12-7

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

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 [ 172103-12-7 ]

CAS No. :172103-12-7
Formula : C9H18O2
M.W : 158.24
SMILES Code : CC(C)CC(C)C(OCC)=O

Safety of [ 172103-12-7 ]

Application In Synthesis of [ 172103-12-7 ]

* 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 [ 172103-12-7 ]

[ 172103-12-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 25415-67-2 ]
  • [ 74-88-4 ]
  • [ 172103-12-7 ]
  • 2
  • [ 23784-96-5 ]
  • [ 172103-12-7 ]
  • ethyl 2-[(5-chloro-2-thienyl)methyl]-2,4-dimethyl-pentanoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
38% To a solution of ethyl 2,4-dimethylpentanoate (0.36 g, 2.28 mmol) in tetrahydrofuran(0.25 M, 9.1 mL) at -70 00 was added a solution of lithium diisopropylamide (2 M in THF, 1.3 equiv., 1.5 mL, 2.96 mmol ). The solution was stirred at -70 00 for 1 h. 2-chloro-5- (chloromethyl)thiophene (1 .3 equiv., 0.37 mL, 2.96 mmol) was then added and the orange solution was allowed to warmup to rt and stirred at this temperature for 16 h. The reactionmixture was quenched with a saturated aqueous solution of NH4CI. The two phases were separated and the aqueous phase was extracted twice with ethyl acetate. The combined organic phase was washed with brine, dried over anhydrous Na2504, filtered and concentrated. Purification of the residue by flash chromatography gave ethyl 2-[(5-chloro-2- thienyl)methyl]-2,4-dimethyl-pentanoate (0.25 g, 38% yield) as a yellow liquid : LC-MS(Method G), Rt = 1.35 mm;1H NMR (400 MHz, CHLOROFORM-d) 6 ppm 0.91 (d, 6H) 1.15 (s, 3H) 1.28 (t, 3H)1.45 (m, 1H) 1.68-1.75 (m, 2H)2.71 (d, 1H) 3.19 (d, 1H)4.14 (q, 2H) 6.52 (d, 1H) 6.70 (d,1 H).
38% To a solution of ethyl 2,4-dimethylpentanoate (0.36 g, 2.28 mmol) in tetrahydrofuran (0.25 M, 9.1 mL) at -70 C was added a solution of lithium diisopropylamide (2 M in THF, 1 .3 equiv., 1.5 mL, 2.96 mmol ). The solution was stirred at -70 C for 1 h. 2-chloro-5- (chloromethyl)thiophene (1 .3 equiv., 0.37 mL, 2.96 mmol) was then added and the orange solution was allowed to warmup to rt and stirred at this temperature for 16 h. The reaction mixture was quenched with saturated aqueous NH4CI solution. The two phases were separated and the aqueous phase was extracted twice with ethyl acetate. The combined organic phase was washed with brine, dried over anhydrous Na2S04, filtered and (0851) concentrated. Purification of the residue by flash chromatography gave ethyl 2-[(5-chloro-2- thienyl)methyl]-2,4-dimethyl-pentanoate (0.25 g, 38% yield) as a yellow liquid : LC-MS (Method G), Rt = 1.35 min; (0852) 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 0.91 (d, 6H) 1.15 (s, 3H) 1.28 (t, 3H) 1 .45 (m, 1 H) 1 .68-1 .75 (m, 21-1) 2.71 (d, 1 H) 3.19 (d, 1 H) 4.14 (q, 2H) 6.52 (d, 1 1-1) 6.70 (d, 1 H).
 

Historical Records