trans-2-Phenylcyclopropylboronic acid

Base Information

• Chemical Name: trans-2-Phenylcyclopropylboronic acid
• CAS No.: 217634-41-8
• Molecular Formula: C₉H₁₁BO₂
• Molecular Weight: 161.996
• DSSTox Substance ID: DTXSID00453759
• Nikkaji Number: J1.046.231B
• Wikidata: Q82274989

Synonyms:TRANS-2-PHENYLCYCLOPROPYLBORONIC ACID;204378-97-2;217634-41-8;((1R,2R)-2-Phenylcyclopropyl)boronic acid;[(1R,2R)-2-phenylcyclopropyl]boronic Acid;starbld0000572;SCHEMBL1781688;DTXSID00453759;JUMGFYYVCWOJDO-DTWKUNHWSA-N;[(1beta)-2alpha-Phenylcyclopropyl]boronic acid;EN300-254325;rac-[(1R,2R)-2-phenylcyclopropyl]boronic acid;Rel-((1R,2R)-2-phenylcyclopropyl)boronic acid;TRANS-1-PHENYL-CYCLOPROPANE-2-BORONIC ACID

Chemical Property of trans-2-Phenylcyclopropylboronic acid

Chemical Property:

• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 162.0852098
• Heavy Atom Count: 12
• Complexity: 155

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: B(C1CC1C2=CC=CC=C2)(O)O
• Isomeric SMILES: B([C@@H]1C[C@H]1C2=CC=CC=C2)(O)O

Technology Process of trans-2-Phenylcyclopropylboronic acid

There total 1 articles about trans-2-Phenylcyclopropylboronic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

C6H5CH(CH2)CHBO2(CHCON(CH3)2)2 + water (7732-18-5) → (1R, 2R)-2-phenylcyclopropylboronic acid (217634-41-8)

Guidance literature:

In not given;

DOI:10.1002/(SICI)1521-3773(19981102)37:20<2845::AID-ANIE2845>3.0.CO;2-U

Reference yield: 93.0%

2,2-Dimethyl-1,3-propanediol (126-30-7) + (1R, 2R)-2-phenylcyclopropylboronic acid (217634-41-8) → 2-n-butyl-5,5-dimethyl-1,3,2-dioxaborinane (879224-89-2)

Guidance literature:

In tetrahydrofuran; for 0.666667h; Dean-Stark; Reflux;

DOI:10.1002/adsc.201400147

Reference yield: 71.0%

2,2-Dimethyl-1,3-propanediol (126-30-7) + (1R, 2R)-2-phenylcyclopropylboronic acid (217634-41-8) → 2-(2-phenylcyclopropyl)-5,5-dimethyl-1,3,2-dioxaborinane

Guidance literature:

In tetrahydrofuran; for 0.666667h; Dean-Stark; Reflux;

DOI:10.1002/adsc.201400147

upstream raw materials:

water

Downstream raw materials:

trans-1-(4-Nitrophenyl)-2-phenylcyclopropan

(1R,2R)-1,2-diphenylcyclopropane

2-n-butyl-5,5-dimethyl-1,3,2-dioxaborinane

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