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BOC-DL-3-AMINOBUTYRIC ACID

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Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: CAS:52815-19-7
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
Company Name: BOC Sciences
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Products Intro: Product Name:N-β-(t-Butoxycarbonyl)-DL-β-aminobutyric acid
CAS:52815-19-7
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Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:3-((tert-Butoxycarbonyl)amino)butanoic acid
CAS:52815-19-7
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-40544
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: CAS:52815-19-7
Purity:0.99 Package:1kg
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Products Intro: Product Name:BOC-DL-3-AMINOBUTYRIC ACID
CAS:52815-19-7
Purity:99.0% Package:1g;1USD

BOC-DL-3-AMINOBUTYRIC ACID manufacturers

BOC-DL-3-AMINOBUTYRIC ACID Basic information
Product Name:BOC-DL-3-AMINOBUTYRIC ACID
Synonyms:3-TERT-BUTOXYCARBONYLAMINO-BUTYRIC ACID;BOC-DL-3-AMINOBUTYRIC ACID;BOC-D,L-BETA-ABU-OH;BOC-DL-BETA-AMINOBUTYRIC ACID;N-BETA-T-BOC-D,L-BETA-AMINOBUTYRIC ACID;3-(tert-butoxycarbonyl)butanoic acid;3-((tert-butoxycarbonyl)amino)butanic acid;Boc-DL-3-aminobutanoic acid
CAS:52815-19-7
MF:C9H17NO4
MW:203.24
EINECS:
Product Categories:pharmacetical
Mol File:52815-19-7.mol
BOC-DL-3-AMINOBUTYRIC ACID Structure
BOC-DL-3-AMINOBUTYRIC ACID Chemical Properties
Melting point 98-100 °C
Boiling point 339.5±25.0 °C(Predicted)
density 1.101±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka4.43±0.10(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HazardClass IRRITANT
MSDS Information
BOC-DL-3-AMINOBUTYRIC ACID Usage And Synthesis
Synthesis
DL-3-Aminobutyric acid

2835-82-7

Di-tert-butyl dicarbonate

24424-99-5

3-t-butoxycarbonylaminobutyric acid

43080-09-7

The general procedure for the synthesis of 3-[[(1,1-dimethylethoxy)carbonyl]amino]butanoic acid from DL-3-aminobutyric acid (CAS No. [541-48-02], 18.72 g, 176.09 mmol) and di-tert-butyl dicarbonate (39.62 g, 176.09 mmol) is as follows: first, DL-3-aminobutyric acid was dissolved in 96 mL of water, followed by the addition of a 76 mL aqueous solution of di-tert-butyl dicarbonate and NaOH (8.03 g, 200.74 mmol), followed by the addition of tert-butanol (132 mL). The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the reaction solution was concentrated under vacuum, then diluted with 200 mL of ethyl acetate and acidified by adjusting to pH 3 with dilute hydrochloric acid. After standing and layering, the aqueous phase was extracted with 200 mL of ethyl acetate. The organic phases were combined, dried with magnesium sulfate, filtered and concentrated in vacuum to give 34.5 g of the target compound as a colorless oil in 82% yield. NMR hydrogen spectrum (300MHz, CDCl3, δ, ppm): 1.25 (d, J = 7.0Hz, 3H); 1.45 (s, 9H); 2.55 (m, 2H); 4.04 (m, 1H); 4.93 (broad peak, 1H); 8.41 (broad peak, 1H).

References[1] Journal of Organic Chemistry, 2001, vol. 66, # 20, p. 6541 - 6544
[2] Organic Letters, 2012, vol. 14, # 1, p. 398 - 401
[3] Patent: WO2017/76998, 2017, A1. Location in patent: Page/Page column 161
[4] Organic Letters, 2005, vol. 7, # 21, p. 4781 - 4784
[5] Synlett, 2004, # 15, p. 2709 - 2712
BOC-DL-3-AMINOBUTYRIC ACID Preparation Products And Raw materials
Raw materialsDL-3-Aminobutyric acid-->TERT-BUTYL FORMATE-->Di-tert-butyl dicarbonate-->Sodium hydroxide-->tert-Butanol
Tag:BOC-DL-3-AMINOBUTYRIC ACID(52815-19-7) Related Product Information
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