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Chemical Structure| 53684-57-4 Chemical Structure| 53684-57-4

Structure of 53684-57-4

Chemical Structure| 53684-57-4

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Product Details of [ 53684-57-4 ]

CAS No. :53684-57-4
Formula : C5H11Cl2NO
M.W : 172.05
SMILES Code : O=C(Cl)C[N+](C)(C)C.[Cl-]
MDL No. :MFCD00270368

Safety of [ 53684-57-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H312-H314-H332
Precautionary Statements:P260-P261-P264-P270-P271-P280-P301+P312-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P321-P322-P330-P363-P405-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 53684-57-4 ]

* 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 [ 53684-57-4 ]

[ 53684-57-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 98-55-5 ]
  • [ 53684-57-4 ]
  • <i>p</i>-menth-1-en-8-yloxycarbonylmethyl-trimethyl-ammonium; chloride [ No CAS ]
  • 2
  • [ 53684-57-4 ]
  • [ 75747-14-7 ]
  • [ 857402-60-9 ]
YieldReaction ConditionsOperation in experiment
57% 17-Allylaminogeldanamycin (1) (113 mg, 0.19 mmol, 1.0 equiv) was dissolved in 2 mL dichloromethane and stirred with a 10% aqueous solution of sodium hydrosulfite (2 mL). The deep purple solution turned yellow after 5 min and the mixture was stirred for an additional 25 min. The organic layer was removed via syringe and the aqueous solution was extracted with an additional 0.30 mL dichloromethane. The combined organic solutions were washed with brine (1.0 mL) and then added directly to a solution of the acid chloride hydrochloride (33 mg, 0.21 mmol, 1.1 equiv) in 0.20 mL dichloromethane. The reaction mixture was stirred for 2 h and poured into a separatory funnel with 3.0 mL water. The organic layer was extracted and then washed with additional 2.0 mL water. The combined aqueous layers were lyophilized to yield 13 as a white fluffy powder (78 mg, 0.11 mmol, 57% yield). The material was analyzed by 1H NMR in CDC13/deuterated DMSO (6: 1) and LC-MS.
57% Example 20: Preparation of N,N,N-Trimethylammonium Acetate Co-Salt of the Hydroquinone of 17- AAG[0092] <strong>[75747-14-7]17-AAG</strong> (113 mg, 0.19 mmol, 1.0 equiv) was dissolved in 2 mL dichloromethane and stirred with a 10% aqueous solution of sodium hydrosulfite (2 mL). The deep purple solution turned yellow after 5 min and the mixture was stirred for an additional 25 min. The organic layer was removed via syringe and the aqueous solution was extracted with an additional 0.30 mL dichloromethane. The combined organic solutions were washed with brine (1.0 mL) and then added directly to a solution of the acid chloride hydrochloride (33 mg, 0.21 mmol, 1.1 equiv) in 0.20 mL dichloromethane. The reaction mixture was stirred for 2 h and poured into a separatory funnel with 3.0 mL water. The organic layer was extracted and then washed with additional 2.0 mL water. The combined aqueous layers were lyophilized to yield 21 as a white fluffy powder (78 mg, 0.11 mmol, 57% yield). The material was analyzed by 1H NMR in CDC^/deuterated DMSO (6:1) and LC-MS.
 

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