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Chemical Structure| 165528-69-8 Chemical Structure| 165528-69-8

Structure of 165528-69-8

Chemical Structure| 165528-69-8

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Product Details of [ 165528-69-8 ]

CAS No. :165528-69-8
Formula : C13H16ClNO4
M.W : 285.72
SMILES Code : O=C(O)C1=CC=C(CNC(OC(C)(C)C)=O)C(Cl)=C1

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Application In Synthesis of [ 165528-69-8 ]

* 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 [ 165528-69-8 ]

[ 165528-69-8 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 24424-99-5 ]
  • [ 74733-30-5 ]
  • [ 165528-69-8 ]
YieldReaction ConditionsOperation in experiment
67% To a saturated solution of ammonia in ethanol (170 ml) was added <strong>[74733-30-5]methyl 4-bromomethyl-3-chlorobenzoate</strong> from Example 4A (5.5 g, 20.9 mmol). The mixture was stirred at room temperature for 1 h and then concentrated in vacuo. The residue was triturated with diethyl ether and the resultant white crystals were filtered off and washed with more diethyl ether. To a solution of this solid in water (100 ml) were added solutions of di-tert-butyl dicarbonate (5.0 g, 23.0 mmol) in dioxan (100 ml) and sodium hydroxide (1.86 g, 46.0 mmol) in water (100 ml). The mixture was stirred at room temperature for 18h and then concentrated in vacuo. The aqueous residue was acidified with citric acid and extracted with chloroform/2-propanol. The organic layer was washed with water, dried over MgSO4, and concentrated in vacuo to give a white solid identified as 4-(tert-butyloxycarbonylaminomethyl)-3-chlorobenzoic acid (2.8 g, 67%).
67% To a saturated solution of ammonia in ethanol (170 ml) was added <strong>[74733-30-5]methyl 4-bromomethyl-3-chlorobenzoate</strong> from Example A1 (5.5 g, 20.9 mmol).. The mixture was stirred at room temperature for 1 h and then concentrated in vacuo.. The residue was triturated with diethyl ether and the resultant white crystals were filtered off and washed with more diethyl ether.. To a solution of this solid in water (100 ml) were added solutions of (BOC)2O (5.0 g, 23.0 mmol) in dioxan (100 ml) and sodium hydroxide (1.86 g, 46.0 mmol) in water (100 ml).. The mixture was stirred at room temperature for 18 h and then concentrated in vacuo.. The aqueous residue was acidified with citric acid and extracted with chloroform/IPA. The organic layer was washed with water, dried over MgSO4, and concentrated in vacuo to give a white solid; yield 2.8 g (67%).
With sodium hydroxide; ammonia; In 1,4-dioxane; ethanol; water; A2. 4-(tert-Butyloxycarbonylaminomethyl)-3-chlorobenzoic acid To a saturated solution of ammonia in ethanol (170 ml) was added <strong>[74733-30-5]methyl 4-bromomethyl-3-chlorobenzoate</strong> from Example A1 (5.5 g, 20.9 mmol). The mixture was stirred at room temperature for 1 h and then concentrated in vacuo. The residue was triturated with diethyl ether and the resultant white crystals were filtered off and washed with more diethyl ether. To a solution of this solid in water (100 ml) were added solutions of (BOC)2O (5.0 g, 23.0 mmol) in dioxan (100 ml) and sodium hydroxide (1.86 g, 46.0 mmol) in water (100 ml). The mixture was stirred at room temperature for 18 h and then concentrated in vacuo. The aqueous residue was acidified with citric acid and extracted with chloroform/IPA. The organic layer was washed with water, dried over MgSO4, and concentrated in vacuo to give a white solid; yield 2.89 (67%).
  • 3
  • (Boc)2O [ No CAS ]
  • [ 74733-30-5 ]
  • [ 165528-69-8 ]
YieldReaction ConditionsOperation in experiment
2.8 g (67%) With sodium hydroxide; ammonia; In 1,4-dioxane; ethanol; water; A2. 4-(tert-Butyloxycarbonylaminomethyl)-3-chlorobenzoic acid To a saturated solution of ammonia in ethanol (170 ml) was added <strong>[74733-30-5]methyl 4-bromomethyl-3-chlorobenzoate</strong> from Example A1 (5.5 g, 20.9 mmol). The mixture was stirred at room temperature for 1 hr and then concentrated in vacuo. The residue was triturated with diethyl ether and the resultant white crystals were fiflered off and washed with more diethyl ether. To a solution of this solid in water (100 ml) were added solutions of (BOC)2O (5.0 g, 23.0 mmol) in dioxan (100 ml) and sodium hydroxide (1.86 g, 46.0 mmol) in water (100 ml). The mixture was stirred at room temperature for 18 h and then concentrated in vacuo. The aqueous residue was acidified with citric acid and extracted with chloroform/IPA. The organic layer was washed with water, dried over MgSO4, and concentrated in vacuo to give a white solid; yield 2.8 g (67%).
 

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