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Chemical Structure| 61676-61-7 Chemical Structure| 61676-61-7

Structure of 61676-61-7

Chemical Structure| 61676-61-7

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Product Details of [ 61676-61-7 ]

CAS No. :61676-61-7
Formula : C9H19BO3
M.W : 186.06
SMILES Code : CC1CC(C)(C)OB(OC(C)C)O1
MDL No. :MFCD15143641
InChI Key :AHCZPHINTQYKPU-UHFFFAOYSA-N
Pubchem ID :12493145

Safety of [ 61676-61-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H226-H318
Precautionary Statements:P280-P305+P351+P338
Class:3
UN#:1993
Packing Group:

Application In Synthesis of [ 61676-61-7 ]

* 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 [ 61676-61-7 ]

[ 61676-61-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 61676-61-7 ]
  • [ 65854-91-3 ]
  • N-[4-chloro-2-(4,4,6-trimethyl-[1,3,2]dioxaborinan-2-yl)-phenyl]-2,2-dimethyl-propionamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
74% General procedure: Preparation of N-[4-chloro-2-(4,4,6-trimethyl-[1,3,2]dioxaborinan-2-yl)-phenyl]-2,2-dimethyl-propionamide (33): To a solution of N-(4-chloro-phenyl)-2,2-dimethyl-propionamide (29) (2.11 g, 10 mmol) in dry THF, n-butyl lithium solution was added dropwise (13 ml, 2.1 equiv, 1.6 M in hexanes) under an argon atmosphere at -40 C. The reaction mixture was stirred for 2 h at 0 C during which time a white precipitate formed. The suspension was cooled to -20 C and neat 2-isopropoxy-4,4,6-trimethyl[1,3,2]dioxaborinane (10) (2.8 g, 15 mmol, 1.5 equiv) was added dropwise. After stirring for 1 h at this temperature, the reaction mixture was allowed to warm up to 0 C and subsequently quenched with a saturated aqueous solution of ammonium chloride (30 ml). The layers were then separated and the water layer was further extracted with dichloromethane (3 × 30 ml). The combined organic layers were dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude residue was purified using flash chromatography on silica gel (15% ethyl acetate: hexanes) to obtain the title compound in 74% yield. 1H NMR (400 MHz, CDCl3): delta 9.62 (s, 1H), 8.50 (d, J = 9.2 Hz, 1H), 7.73 (d, J = 2.5 Hz, 1H), 7.26 (dd, J = 8.8 Hz, J = 2.7 Hz, 1H), 4.39 (m, 1H), 1.87 (dd, J = 13.5 Hz, J = 2.9 Hz, 1H), 1.63 (t, J = 2.5 Hz, 1H), 1.40 (d, J = 10.7 Hz, 6H), 1.36 (d, J = 6.7 Hz, 3H), 1.29 (s, 9H). 11B NMR (128.3 MHz, CDCl3): delta 26.2. 13C NMR (100.6 MHz, CDCl3): delta 177.0, 143.1, 134.9, 131.1, 127.3, 120.5, 75.5, 65.8, 45.5, 39.6, 31.1, 28.0, 27.5, 23.0.
74% Synthesis of N-[4-Chloro-2-(4,4,6-trimethyl-[1,3,2]dioxaborinan-2-yl)-phenyl]-2,2-dimethyl-propionamide To a solution of N-(4-chloro-phenyl)-2,2-dimethyl-propionamide (2.11 g, 10 mmol) in dry THF, n-butyl lithium solution was added dropwise (13 ml, 2.1 eq., 1.6 M in hexanes) under an argon atmosphere at -40 C. The reaction mixture was stirred for 2 hours at 0 C. during which time a white precipitate formed. The suspension was cooled to -20 C. and neat 2-isopropoxy-4,4,6-trimethyl-[1,3,2]dioxaborinane (2.8 g, 15 mmol, 1.5 eq.) was added dropwise. After stirring for 1 hour at this temperature, the reaction mixture was allowed to warm up to 0 C. and subsequently quenched with an aqueous solution of ammonium chloride (30 ml). The layers were then separated and the water layer was further extracted with dichloromethane (3*30 ml). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and evaporated under reduced pressure. The crude residue was purified using flash chromatography on silica gel (15% ethyl acetate:hexanes) to obtain the title compound in good yield (74%). 1H NMR (400 MHz, CDCl3): delta 9.62 (s, 1H), 8.50 (d, J=9.2 Hz, 1H), 7.73 (d, J=2.5 Hz, 1H), 7.26 (dd, J=8.8 Hz, J=2.7 Hz, 1H), 4.39 (m, 1H), 1.87 (dd, J=13.5 Hz, J=2.9 Hz, 1H), 1.63 (t, J=2.5 Hz, 1H), 1.40 (d, J=10.7 Hz, 6H), 1.36 (d, J=6.7 Hz, 3H), 1.29 (s, 9H). 11B NMR (128.3 MHz, CDCl3): delta 26.2. 13C NMR (100.6 MHz, CDCl3): delta 177.0, 143.1, 134.9, 131.1, 127.3, 120.5, 75.5, 65.8, 45.5, 39.6, 31.1, 28.0, 27.5, 23.0.
 

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