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Chemical Structure| 109347-40-2 Chemical Structure| 109347-40-2

Structure of 109347-40-2

Chemical Structure| 109347-40-2

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Product Details of [ 109347-40-2 ]

CAS No. :109347-40-2
Formula : C8H7BrO
M.W : 199.04
SMILES Code : BrC1=CC=CC(CC=O)=C1
MDL No. :MFCD02261727
InChI Key :GQPCWVVXGHFKQY-UHFFFAOYSA-N
Pubchem ID :20387554

Safety of [ 109347-40-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P264-P302+P352-P304+P340-P305+P351+P338-P332+P313-P337+P313

Application In Synthesis of [ 109347-40-2 ]

* 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 [ 109347-40-2 ]

[ 109347-40-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-91-8 ]
  • [ 109347-40-2 ]
  • [ 364793-86-2 ]
YieldReaction ConditionsOperation in experiment
35% With sodium tris(acetoxy)borohydride; In dichloromethane; at 20.0℃; for 1.0h; To a stirred solution of 2-(3-bromophenyl)acetaldehyde (400 mg, 2.01 mmol) in dry CH2Cl2(10 mL) was added morpholine (175 mg, 2.01 mmol). After 10 min, sodiumtriacetoxyborohydride (424 mg, 2.0 mmol) was added and the reaction mixture was stirred atroom temperature for 1 h, it was then washed with a saturated bicarbonate solution, dried, andconcentrated in vacuo. The crude product was filtered through an isolute SCX-2 cartridgethen purified on a silica column eluting with 3% [7 M NH3 in MeOH] in CH2Cl2 to afford thetitle compound (190 mg, 35%).
 

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• Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blanc Chloromethylation • Bucherer-Bergs Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • Friedel-Crafts Reaction • General Reactivity • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Julia-Kocienski Olefination • Kinetics of Alkyl Halides • Knoevenagel Condensation • Kumada Cross-Coupling Reaction • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Dihalides • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Stetter Reaction • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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