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Chemical Structure| 885609-88-1 Chemical Structure| 885609-88-1

Structure of 885609-88-1

Chemical Structure| 885609-88-1

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Product Details of [ 885609-88-1 ]

CAS No. :885609-88-1
Formula : C12H16ClNO2
M.W : 241.71
SMILES Code : CC(C(=O)NC1C(CO)=CC=C(Cl)C=1)(C)C
MDL No. :N/A

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Application In Synthesis of [ 885609-88-1 ]

* 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 [ 885609-88-1 ]

[ 885609-88-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 37585-16-3 ]
  • [ 3282-30-2 ]
  • [ 885609-88-1 ]
YieldReaction ConditionsOperation in experiment
100% With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; at 0℃; for 0.5h; N-(5-Chloro-2-(hydroxymethyl)phenyl)pivalamide. Trimethylacetyl chloride (0.72 mL, 5.82 mmol) was fast dropwise added to <strong>[37585-16-3](2-amino-4-chlorophenyl)methanol</strong> (874 mg, 5.55 mmol) in CH2Cl2 (20 mL) and THF (6 mL) at 0 C., and followed by the addition of DIEA (2.41 mL, 13.9 mmol). The resulting mixture was stirred for 30 min. Then the mixture was partitioned between saturated NaHCO3 (50 mL) and CH2Cl2 (100 mL). After separation, the organic phase was washed with brine (30 mL), dried on MgSO4, and concentrated on rotary vacuum to afford the expected crude product (1.34, 100% yield), which was pure enough to be used in next step. Mass spec. 242.08 (MH+), Calc. for C12H16ClNO2 241.09.
100% With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; at 0℃; for 0.5h; N-(5-Chloro-2-(hydroxymethyl)phenyl)pivalamide; Trimethylacetyl chloride (0.72 mL, 5.82 mmol) was fast dropwise added to <strong>[37585-16-3](2-amino-4-chlorophenyl)methanol</strong> (874 mg, 5.55 mmol) in CH2Cl2 (20 mL) and THF(6mL) at 0 C., and followed by the addition of DIEA (2.41 mL, 13.9 mmol). The resulting mixture was stirred for 30 min. Then the mixture was partitioned between saturated NaHCO3 (50 mL) and CH2Cl2 (100 mL). After separation, the organic phase was washed with brine (30 mL), dried on MgSO4, and concentrated on rotary vacuum to afford the expected crude product (1.34, 100% yield), which was pure enough to be used in next step. Mass spec. 242.08 (MH+), Calc. for C12H16ClNO2 241.09.
 

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