| Identification | Back Directory | [Name]
[(1S)-2-[[(tert-Butyl)diMethylsilyl]oxy]-1-(hydroxyMethyl)ethyl]-carbaMic Acid tert-Butyl Ester | [CAS]
185692-85-7 | [Synonyms]
(S)-Tert-Butyl (1-((Tert-Butyldimethylsilyl)Oxy)-3-Hydroxypropan-2-Yl)Carbamate tert-butyl (S)-(1-((tert-butyldimethylsilyl)oxy)-3-hydroxypropan-2-yl)carbamate tert-butyl N-[(2S)-1-[tert-butyl(dimethyl)silyl]oxy-3-hydroxypropan-2-yl]carbamate [(1S)-2-[[(tert-Butyl)diMethylsilyl]oxy]-1-(hydroxyMethyl)ethyl]-carbaMic Acid tert-Butyl Ester Carbamic acid, N-[(1S)-2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester | [Molecular Formula]
C14H31NO4Si | [MDL Number]
MFCD28403204 | [MOL File]
185692-85-7.mol | [Molecular Weight]
305.49 |
| Chemical Properties | Back Directory | [Boiling point ]
377.3±37.0 °C(Predicted) | [density ]
0.979±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Oil | [pka]
11.57±0.46(Predicted) | [color ]
Pale Yellow |
| Hazard Information | Back Directory | [Chemical Properties]
Pale Yellow Oil | [Uses]
Intermediate in the synthesis of Chloramphenicol (C325030). | [Synthesis]
The general procedure for the synthesis of tert-butyl (S)-((1-((tert-butyldimethylmethylsilyl)oxy)-3-hydroxypropan-2-yl)carbamate, using the compound (CAS:112418-19-6) as a starting material, was as follows: to a solution of tetrahydrofuran (THF, 150 ml) of the product obtained in step 3 (16.5 g, 45.6 mmol) was slowly added a 2 M THF solution of lithium borohydride (37.1 ml). The reaction mixture was stirred at room temperature for 2.5 hours. After completion of the reaction, the reaction was quenched with saturated ammonium chloride (NH4Cl) solution and extracted with ethyl acetate (EtOAc, 2 x 250 ml). The combined organic layers were washed sequentially with saturated ammonium chloride solution (100 ml), saturated sodium bicarbonate solution and brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the target product (14.5 g, 100% yield). Mass spectrometry (MS) analysis showed m/e 306 (M + H)+. | [References]
[1] Patent: WO2006/14762, 2006, A1. Location in patent: Page/Page column 42 [2] Patent: WO2006/14944, 2006, A1. Location in patent: Page/Page column 32 [3] European Journal of Organic Chemistry, 2013, # 31, p. 7145 - 7151 [4] Journal of Medicinal Chemistry, 2015, vol. 58, # 10, p. 4204 - 4219 [5] Patent: WO2008/86122, 2008, A2. Location in patent: Page/Page column 68 |
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Struchem Co., Ltd.
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0512-63009836 18994340901 |
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http://www.beidapharma.com |
| Company Name: |
Energy Chemical
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021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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