Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Carboxylic acids and derivatives >  Cyclic carboxylic acids >  H-GAMMA-ABU-OBZL P-TOSYLATE

H-GAMMA-ABU-OBZL P-TOSYLATE

Basic information Safety Supplier Related

H-GAMMA-ABU-OBZL P-TOSYLATE Basic information

Product Name:
H-GAMMA-ABU-OBZL P-TOSYLATE
Synonyms:
  • H-GAMMA-ABU-OBZL P-TOSYLATE
  • H-GAMMA-ABU-OBZL TOS-OH
  • H-ABU(4)-OBZL TOS-OH
  • GAMMA-AMINOBUTYRIC ACID BENZYL ESTER P-TOSYLATE
  • GAMMA-AMINOBUTYRIC ACID-OBZL P-TOSYLATE
  • γ-Aminobutyric acid benzyl ester p-tosylate
  • Hγ-Abu-OBzl·p-tosylate
  • H-g-Abu-OBzl·TosOH
CAS:
26727-22-0
MF:
C18H23NO5S
MW:
365.44
Mol File:
26727-22-0.mol
More
Less

H-GAMMA-ABU-OBZL P-TOSYLATE Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
More
Less

H-GAMMA-ABU-OBZL P-TOSYLATE Usage And Synthesis

Synthesis

104-15-4

100-51-6

56-12-2

26727-22-0

A suspension of γ-aminobutyric acid (GABA) (3.50 g, 0.034 mol), benzyl alcohol (7.30 g, 7 mL, 0.068 mol), and p-toluenesulfonic acid monohydrate (PTSA) (7.10 g, 0.037 mol) was heated to reflux for 5 hr in toluene (200 mL), and the resulting water was removed by azeotropic distillation. Upon completion of the reaction, the mixture was concentrated to one-third of the original volume and the product was subsequently precipitated by the addition of ether (100 mL). The precipitate was collected by filtration, dissolved in methanol (60 mL) and reprecipitated by adding ether (100 mL) again. After filtration, it was dried to obtain 4-methylbenzenesulfonate, 4-aminobutyric acid benzyl ester (12.30 g, 99% yield) in the form of white crystals. The melting point of the product was 106.2-106.7 °C (determined in ether); Infrared spectrum (ATR): 3100, 3039, 2942, 1732, 1642, 1532, 1188, 1125 cm^-1; ^1H NMR (200 MHz, CD3OD): δ = 7.71 (d, J = 8.0 Hz, 2H, HPTSA), and 7.37-7.30 (m, 5H, HCAr), 7.20 (d, J=8.4 Hz, 2H, HPTSA), 5.11 (s, 2H, H2CBn), 2.95 (t, J=7.5 Hz, 2H, H2C(4)GABA), 2.47 (t, J=7.3 Hz, 2H, H2C(2)GABA), 2.33 (s 3H, H3CPTSA), 1.92 (quint, J=7.4 Hz, 2H, H2C(3)GABA) ppm; ^13C NMR (50 MHz, CD3OD): δ=173.83 (CO2Bn), 143.35, 141.82, 137.43, 129.91, 129.59, 129.30, 126.91 (CAr), 67.44 (CH2Bn), 40.00 (CH2(4)GABA), 31.59 (CH2(2)GABA), 23.65 (CH2(3)GABA), 21.30 (CH3PTSA) ppm; Mass Spectra (ESI): calculated values of C11H16NO2 ([M+H]+): 194.1181, measured value: 194.1167.

References

[1] Tetrahedron, 2017, vol. 73, # 50, p. 7073 - 7078
[2] Organic and Biomolecular Chemistry, 2009, vol. 7, # 11, p. 2327 - 2337
[3] RSC Advances, 2015, vol. 5, # 81, p. 66339 - 66354
[4] Patent: WO2014/59158, 2014, A1. Location in patent: Page/Page column 38-39
[5] Tetrahedron Letters, 2015, vol. 56, # 48, p. 6803 - 6806

H-GAMMA-ABU-OBZL P-TOSYLATESupplier

Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Chemsky (shanghai) International Co.,Ltd
Tel
021-50135380
Email
shchemsky@sina.com
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Email
waley188@sohu.com
NINGBO INNO PHARMCHEM CO.,LTD.
Tel
86-574-27787657
Email
info@dearchem.com
Shanghai GL Peptide Ltd.
Tel
+86-21-61263340; 17609490614 13764994101
Email
fisherwang@glschina.com