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(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE

(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE ??? ???
?? ??:
119838-44-7
???:
(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE
???(??):
R-BOC-BMI;(R)-(+)-1-(TERT-BUTOXYCARBONYL)-2-T-BUT&;(R)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE;(R)-1-Boc-2-tert-butyl-3-methylimidazolidin-4-one;(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE;(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE 99%;N-(tert-butoxycarbonyl)-2-butyl-3-methyl-4-imidazolidinone;t-Butyl 2-t-Butyl-3-methyl-4-oxo-1-imidazolidinecarboxylate;(R)-1-Boc-2-tert-butyl-3-methyl-4-imidazolidinone≥ 99% (Titration);(R)-(+)-1-(TERT-BUTOXYCARBONYL)-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINE
CBNumber:
CB9166082
???:
C13H24N2O3
??? ??:
256.34
MOL ??:
119838-44-7.mol

(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE ??

???
68-70 °C(lit.)
?? ?
399.58°C (rough estimate)
??
1.0600 (rough estimate)
???
1.4365
?? ??
Sealed in dry,2-8°C
?? ?? (pKa)
-0.60±0.40(Predicted)
??? ??
crystalline solid
??
colorless

??

????? 22-24/25
WGK ?? 3
F ?????? 8-10
HS ?? 29332100

(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE C??? ??, ??, ??

??? ??

white crystalline powder

??

(R)-(+)-1-Boc-2-tert-butyl-3-methyl-4-imidazolidinone is a chiral glycine derivative used for the synthesis of amino acids.

Synthesis

The commercial glycine N-methylamide hydrochloride is converted to the racemic imidazolidinone (2) by imine formation with Pivalaldehyde and cyclization under acidic conditions (eq 1). The mandelate salt of like configuration is less soluble and is used for highly efficient resolution; subsequent treatment with Boc anhydride (Di-t-butyl Dicarbonate) gives the enantiomeric Boc-BMI (1) (eq 2).
(R)-( )-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE

(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE ?? ?? ? ???

???

?? ??


(R)-(+)-1-BOC-2-TERT-BUTYL-3-METHYL-4-IMIDAZOLIDINONE ?? ??

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