Home Cart Sign in  
Chemical Structure| 59812-35-0 Chemical Structure| 59812-35-0

Structure of 59812-35-0

Chemical Structure| 59812-35-0

*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 [ 59812-35-0 ]

CAS No. :59812-35-0
Formula : C11H9ClO3S
M.W : 256.71
SMILES Code : O=C(C1=C(Cl)C2=CC=C(OC)C=C2S1)OC
MDL No. :MFCD00620636

Safety of [ 59812-35-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330-P501

Application In Synthesis of [ 59812-35-0 ]

* 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 [ 59812-35-0 ]

[ 59812-35-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 59812-35-0 ]
  • [ 14659-58-6 ]
  • (3-chloro-6-methoxybenzo[b]thiophen-2-yl)(4-fluoro-2,6-dimethylphenyl)methanone [ No CAS ]
YieldReaction ConditionsOperation in experiment
9.8 g With n-butyllithium; In Step 1, 100 grams of Compound 32 was dissolved thionyl chloride and pyridine. Methanol was added to the solution to afford Compound 33. Compound 33 was recrystallized to obtain 50 grams of pure product. The H-NMR was clean. In Step 2, 25 grams of Compound 32 was subjected to 1.3 eq of n-butyl lithium and Compound 34. After column purification 9.8 grams of pure Compound 35 was isolated. The H-NMR was clean. In Step 3, 3.5 grams of Compound 35 was reacted with Boc-anhydride in the presence of triethylamine to afford 5 grams of Compound 37 after work-up and purification. In Step 4, 4.5 grams of Compound 37 was dissolved in DMF and then Cesium Carbonate and Compound 35 were added to afford Compound 38. Compound 38 was purified by column chromatography to afford 6.8 grams of pure compound. H-NMR was clean and HPLC purity was 96%. In Step 5, to a solution of 6.2 grams of Compound 38 in DMF was added iodoethane and sodium hydride. After work-up and column purification 4.4 grams of Compound 39 was isolated. H-NMR was clean. In Step 6, 2 grams of Compound 39 was exposed to BBr3 to afford Compound 100. H-NMR was clean. HPLC purity was 96.5%.
9.8 g With n-butyllithium; Scheme 8 In Step 1, 100 grams of Compound 32 was dissolved in thionyl chloride and pyridine. Methanol was added to the solution to afford Compound 33. Compound 33 was recrystallized to obtain 50 grams of pure product. The H-NMR was clean. In Step 2, 25 grams of Compound 33 were subjected to 1.3 eq of n-butyl lithium and Compound 34. After column purification, 9.8 grams of pure Compound 35 was isolated. The H-NMR was clean. In Step 3, 50 grams of Compound 35 benzyl bromide to afford 61.6 grams of Compound 37. In Step 5, Compound 37 was then mixed with Compound 38 and cesium carbonate in DMSO to afford Compound 39. In Step 6, the benzyl protecting group of Compound 39 was removed by hydrogenation to afford Compound 100.
 

Historical Records

Technical Information

Categories