Basic information Safety Supplier Related

tert-butyl N-[3,3-difluoro-1-(hydroxymethyl)cyclobutyl]carbamate

Basic information Safety Supplier Related

tert-butyl N-[3,3-difluoro-1-(hydroxymethyl)cyclobutyl]carbamate Basic information

Product Name:
tert-butyl N-[3,3-difluoro-1-(hydroxymethyl)cyclobutyl]carbamate
Synonyms:
  • tert-butyl N-[3,3-difluoro-1-(hydroxymethyl)cyclobutyl]carbamate
  • tert-Butyl (3,3-difluoro-1-(hydroxymethyl)cyclobutyl)carbamate
  • 1-(Boc-amino)-3,3-difluorocyclobutane-1-methanol
  • Carbamic acid, N-[3,3-difluoro-1-(hydroxymethyl)cyclobutyl]-, 1,1-dimethylethyl ester
  • DIFLUOROCYCLOBUTANE-1- METHANOL
  • 1-(Boc-amino)-3,3-difluorocyclobutyl]methanol
CAS:
1232365-42-2
MF:
C10H17F2NO3
MW:
237.24
Mol File:
1232365-42-2.mol
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tert-butyl N-[3,3-difluoro-1-(hydroxymethyl)cyclobutyl]carbamate Chemical Properties

storage temp. 
2-8°C
Appearance
yellow solid
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Safety Information

HS Code 
2924297099
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tert-butyl N-[3,3-difluoro-1-(hydroxymethyl)cyclobutyl]carbamate Usage And Synthesis

Uses

1-(Boc-amino)-3,3-difluorocyclobutane-1-methanol is used in preparation of Amide derivatives useful in the treatment of HBV infection or HBV-induced diseases.

Synthesis

1232365-41-1

1232365-42-2

The general procedure for the synthesis of tert-butyl (3,3-difluoro-1-(hydroxymethyl)cyclobutyl)carbamate from compound BB2-g (CAS: 1232365-41-1, 4 g, 0.0143 mol) was as follows: a 2 M lithium borohydride solution (30 mL) was slowly added to an anhydrous THF (100 mL) solution of compound BB2-g under ice bath cooling. The reaction mixture was then gradually warmed to room temperature. The reaction mixture was stirred continuously for 3 hours at room temperature. Upon completion of the reaction, the reaction was quenched by careful addition of ice water and 5% citric acid solution and then extracted three times with dichloromethane (DCM). The organic phases were combined, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to afford the target product tert-butyl (3,3-difluoro-1-(hydroxymethyl)cyclobutyl)carbamate (3.1 g, 91% yield).

References

[1] Patent: WO2010/70615, 2010, A1. Location in patent: Page/Page column 28; 30
[2] Patent: WO2011/70539, 2011, A1. Location in patent: Page/Page column 24; 26
[3] Patent: WO2011/70541, 2011, A1. Location in patent: Page/Page column 25
[4] Patent: WO2011/158197, 2011, A1. Location in patent: Page/Page column 31
[5] Patent: WO2012/172473, 2012, A1. Location in patent: Page/Page column 22

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