2-Propanol, 1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, benzoate, (S)-

Base Information

• Chemical Name: 2-Propanol, 1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, benzoate, (S)-
• CAS No.: 113534-14-8
• Molecular Formula: C16H26O3Si
• Molecular Weight: 294.466
• DSSTox Substance ID: DTXSID301153504
• Mol file: 113534-14-8.mol

Synonyms:113534-14-8;DTXSID301153504;2-Propanol, 1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, benzoate, (S)-

Chemical Property of 2-Propanol, 1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, benzoate, (S)-

Chemical Property:

• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 294.16512122
• Heavy Atom Count: 20
• Complexity: 314

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CO[Si](C)(C)C(C)(C)C)OC(=O)C1=CC=CC=C1
• Isomeric SMILES: C[C@@H](CO[Si](C)(C)C(C)(C)C)OC(=O)C1=CC=CC=C1

Technology Process of 2-Propanol, 1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, benzoate, (S)-

There total 3 articles about 2-Propanol, 1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, benzoate, (S)- 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:

(2S)-1-{[(1,1-dimethylethyl)dimethylsilyl]oxy}-2-propanol (113534-13-7) + benzoyl chloride (98-88-4) → (S)-1-(tert-butyldimethylsiloxy)-2-(benzoyloxy)propane (113534-14-8)

Guidance literature:

DOI:10.1016/S0040-4039(00)98065-1

Reference yield:

C22H33NO4Si (131429-78-2,131429-79-3) → (S)-1-(tert-butyldimethylsiloxy)-2-(benzoyloxy)propane (113534-14-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 1) O₃ 2) NaBH₄

With sodium tetrahydroborate; ozone;

DOI:10.1016/S0040-4039(00)98065-1

Reference yield:

[(1R)-2-hydroxy-1-methyl-ethyl]benzoate (113566-74-8) + tert-butyldimethylsilyl chloride (18162-48-6) → (S)-1-(tert-butyldimethylsiloxy)-2-(benzoyloxy)propane (113534-14-8)

Guidance literature:

DOI:10.1016/S0040-4039(00)98065-1

upstream raw materials:

(2S)-1-{[(1,1-dimethylethyl)dimethylsilyl]oxy}-2-propanol

benzoyl chloride

[(1R)-2-hydroxy-1-methyl-ethyl]benzoate

tert-butyldimethylsilyl chloride

Downstream raw materials:

(S)-1-hydroxypropan-2-yl benzoate