Basic information Safety Supplier Related

BOC-3-AMINOBENZYLALCOHOL

Basic information Safety Supplier Related

BOC-3-AMINOBENZYLALCOHOL Basic information

Product Name:
BOC-3-AMINOBENZYLALCOHOL
Synonyms:
  • TERT-BUTYL 3-(HYDROXYMETHYL)PHENYLCARBAMATE
  • BOC-3-AMINOBENZYLALCOHOL
  • 3-(Boc-aMino)benzyl alcohol
  • ert-Butyl (3-(hydroxymethyl)phe nyl)carbamate
  • Carbamic acid, N-[3-(hydroxymethyl)phenyl]-, 1,1-dimethylethyl ester
  • tert-butyl N-[3-(hydroxymethyl)phenyl]carbamate
  • N-Boc-3-hydroxymethylaniline
CAS:
118684-31-4
MF:
C12H17NO3
MW:
223.27
Mol File:
118684-31-4.mol
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BOC-3-AMINOBENZYLALCOHOL Chemical Properties

Melting point:
98 °C(Solv: hexane (110-54-3); ethyl acetate (141-78-6))
Boiling point:
309.3±25.0 °C(Predicted)
Density 
1.161±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
13.71±0.70(Predicted)
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BOC-3-AMINOBENZYLALCOHOL Usage And Synthesis

Synthesis

24424-99-5

1877-77-6

118684-31-4

Synthesis of Compound 14A: 3-Aminobenzyl alcohol (3 g, 24.36 mmol, 1.00 eq.) was dissolved in tetrahydrofuran (60 mL) followed by addition of di-tert-butyl dicarbonate (6.38 g, 29.23 mmol, 1.20 eq.). The reaction mixture was stirred at room temperature overnight and then diluted with 200 mL of water. It was extracted three times with ethyl acetate (100 mL), the organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give a yellow oily crude product (13.85 g, compound 14A).

References

[1] Patent: WO2016/134450, 2016, A1. Location in patent: Page/Page column 92-93
[2] Patent: WO2017/210471, 2017, A1. Location in patent: Paragraph 0011336; 001137
[3] Patent: US2008/21032, 2008, A1. Location in patent: Page/Page column 56
[4] Patent: US2018/312497, 2018, A1. Location in patent: Paragraph 0066; 0121
[5] Patent: US2012/94997, 2012, A1. Location in patent: Page/Page column 104-105

BOC-3-AMINOBENZYLALCOHOLSupplier

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