Home Cart Sign in  
Chemical Structure| 175204-89-4 Chemical Structure| 175204-89-4

Structure of 175204-89-4

Chemical Structure| 175204-89-4

*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 [ 175204-89-4 ]

CAS No. :175204-89-4
Formula : C9H7F3O4
M.W : 236.14
SMILES Code : O=C(OC)C1=CC(OC(F)(F)F)=CC=C1O
MDL No. :MFCD00219949

Safety of [ 175204-89-4 ]

Application In Synthesis of [ 175204-89-4 ]

* 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 [ 175204-89-4 ]

[ 175204-89-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 67-56-1 ]
  • [ 129644-57-1 ]
  • [ 175204-89-4 ]
YieldReaction ConditionsOperation in experiment
100% With sulfuric acid; at 120℃; for 1.0h;Microwave irradiation; A mixture of 2 -hydroxy-5 - (trifluoromethoxy)benzoic acid (300 mg, 1.35 mmol) and a few drops of concentrated H2SO4 was heated to 120 C for 1 h under microwave irradiation, after which LC-MS analysis showed completion. Reaction mixture was concentrated to dryness to afford methyl 2 -hydroxy-5 -(trifluoromethoxy)benzoate (319 mg, 100 % yield) as a white solid, which was used without further purification. NMR (400 MHz, DMSO-ck) d 10.57 (s, 1H), 7.65 (d, J= 3.2 Hz, 1H), 7.54 (dt, J= 9.4, 3.0 Hz, 1H), 7.10 (d, J= 9.1 Hz, 1H), 3.89 (s, 3H). 19F NMR (376 MHz, DMSO-ifc) d -57.17 (s, 3F). LCMS RT (Method 2) = 3.507 min.
100% With sulfuric acid; at 120℃; for 1.0h;Microwave irradiation; A mixture of 2 -hydroxy-5 - (trifluoromethoxy)benzoic acid (300 mg, 1.35 mmol) and a few drops of concentrated H2SO4 was heated to 120 C for 1 h under microwave irradiation, after which LC-MS analysis showed completion. Reaction mixture was concentrated to dryness to afford methyl 2 -hydroxy-5 -(trifluoromethoxy)benzoate (319 mg, 100 % yield) as a white solid, which was used without further purification. NMR (400 MHz, DMSO-ck) d 10.57 (s, 1H), 7.65 (d, J= 3.2 Hz, 1H), 7.54 (dt, J= 9.4, 3.0 Hz, 1H), 7.10 (d, J= 9.1 Hz, 1H), 3.89 (s, 3H). 19F NMR (376 MHz, DMSO-ifc) d -57.17 (s, 3F). LCMS RT (Method 2) = 3.507 min.
97.8% With sulfuric acid;Heating / reflux; Step 3: Preparation of methyl 2-hvdroxy-5-(trifluoromethoxy)benzoate; Concentrated sulfuric acid (1.0 mL) was carefully added to a solution of 2-hydroxy- 5-trifluoromethoxy-benzoic acid (11.0 g, 49.52 mmol) in methanol (150 mL). The mixture was refluxed overnight. Additional sulfuric acid (1.0 mL) was added and the mixture was refluxed for another 3 days. The mixture was cooled to rt, concentrated and purified by a silica gel plug eluting with hexanes. After concentrating the desired fractions, colorless oil was obtained as pure product (11.4 g, 97.8%). 1H NMR (400 MHz, DMSO-d6) δ 10.80 (IH, s), 7.61 (IH, s), 7.44-7.46 (IH, d, J = 8.0 Hz), 7.01-7.03 (IH, d, J = 8.0 Hz), 3.88 (3H, s); LC-MS m/z 234.9 [(M-H)-], HPLC RT (min) 5.05 {method (A)}.
63% With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 - 20℃; To a round bottom flask containing a magnetic stir bar was added 2-hydroxy-5- (trifluoromethoxy)benzoic acid (2000.0 mg, 9.00 mmol), followed by CH2CI2(30.0 mL)/MeOH (30.0 mL). Using an ice bath, the mixture was cooled to 0 C while stirring. To this reaction mixture was added EDCI (2590.0 mg, 13.5 mmol, 1.5 eq), followed by DMAP (220.0 mg, 1.80 mmol, 0.2 eq). The reaction temperature was allowed to increase up to room temperature while stirring overnight. Upon completion by LCMS analysis, the reaction mixture was concentrated under reduced pressure. The reaction mixture was partitioned between CH2CI2(30.0 mL) and H2O (20.0 mL). The product was extracted with CH2CI2(3 x 30.0 mL) and the combined organics were dried over Na2S04, filtered, and concentrated under reduced pressure. Purification by ISCO flash chromatography (0- 100% EtOAc in hexanes) afforded methyl 2-hydroxy-5-(trifluoromethoxy)benzoate (1356.1 mg, 5.74 mmol, 63%). LCMS (Method A) tR= 1.62 min, m/z = 237.2 [M+H]+.

  • 2
  • [ 129644-57-1 ]
  • [ 18107-18-1 ]
  • [ 175204-89-4 ]
YieldReaction ConditionsOperation in experiment
In methanol; dichloromethane; at 0 - 25℃; for 3.0h; a) Methyl 2-hydroxy-5-(trifluoromethoxy)benzoate To a solution of <strong>[129644-57-1]2-hydroxy-5-(trifluoromethoxy)benzoic acid</strong> (2.2 g, 9.90 mmol) in dichloromethane (10 mL) and methanol (2 mL) at 0 C. was added tms-diazomethane (2M) (5 mL) dropwise and the solution was stirred for 3 h at 25 C. The reaction was then quenched by the addition of water. The resulting solution was extracted with DCM (3*10 mL) and the organic layers combined and concentrated under vacuum. The resulting residue was purified on a silica gel column with ethyl acetate/petroleum ether (10/90). The collected fractions were combined and concentrated under vacuum to yield methyl 2-hydroxy-5-(trifluoromethoxy)benzoate as colorless oil.
 

Historical Records