BOC-DL-2-AMINOBUTYRIC ACID
- Product Name
- BOC-DL-2-AMINOBUTYRIC ACID
- CAS No.
- 77284-64-1
- Chemical Name
- BOC-DL-2-AMINOBUTYRIC ACID
- Synonyms
- Boc-DL-2-Abu;Boc-2-aMinobutyric acid;DL-Boc-Aminobutyric acid;2-(Boc-amino)butyric Acid;BOC-DL-2-AMINOBUTYRIC ACID;2-(tert-butoxycarbonyl)butanoic acid;2-Aminobutanoic acid, N-BOC protected;2-[(tert-Butoxycarbonyl)amino]butanoic acid;(2R)-2-[(tert-butoxycarbonyl)amino]butanoate;Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-
- CBNumber
- CB1146853
- Molecular Formula
- C9H17NO4
- Formula Weight
- 203.24
- MOL File
- 77284-64-1.mol
BOC-DL-2-AMINOBUTYRIC ACID Property
- Melting point:
- 60-62 °C
- Boiling point:
- 334.5±25.0 °C(Predicted)
- Density
- 1.101±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 4.00±0.10(Predicted)
- Appearance
- White to off-white Solid
Safety
- HazardClass
- IRRITANT
- HS Code
- 2922498590
N-Bromosuccinimide Price
- Product number
- B699680
- Product name
- 2-[(tert-Butoxycarbonyl)amino]butanoicAcid
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- AS87974
- Product name
- Boc-2-aminobutyric acid
- Purity
- 95+%
- Packaging
- 5G
- Price
- $86
- Updated
- 2021/12/16
- Product number
- 048298
- Product name
- 2-[(tert-Butoxycarbonyl)amino]butanoic acid
- Purity
- >95%
- Packaging
- 500mg
- Price
- $112
- Updated
- 2021/12/16
- Product number
- 4158-1-14
- Product name
- 2-Aminobutanoic acid, N-Boc protected
- Packaging
- 500mg
- Price
- $184
- Updated
- 2021/12/16
- Product number
- 048298
- Product name
- 2-[(tert-Butoxycarbonyl)amino]butanoic acid
- Purity
- >95%
- Packaging
- 1g
- Price
- $205
- Updated
- 2021/12/16
BOC-DL-2-AMINOBUTYRIC ACID Chemical Properties,Usage,Production
Synthesis
24424-99-5
2835-81-6
77284-64-1
General procedure for the synthesis of N-Boc-DL-2-aminobutyric acid from di-tert-butyl dicarbonate and DL-2-aminobutyric acid: 10 g (96.97 mmol, 1.0 eq.) of DL-2-aminobutyric acid was dissolved in 65 mL of methanol to which 97 mL of sodium hydroxide (NaOH) solution was added. Subsequently, 25.4 g (116.37 mmol, 1.2 eq.) of di-tert-butyl dicarbonate (Boc2O) was slowly added at 0 °C. The reaction mixture was stirred at room temperature for 48 h. After completion of the reaction, it was concentrated under reduced pressure. The concentrated reaction mixture was adjusted pH to 2-3 with 1N HCl and then extracted with ethyl acetate. The organic layer was separated, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by column chromatography (SiO2, eluent gradient: hexane/ethyl acetate, 10:1 to hexane/ethyl acetate, 3:1) to afford 18.5 g of N-Boc-DL-2-aminobutyric acid (2-((tert-butoxycarbonyl)amino)butyric acid) as a colorless oil (91.02 mmol, 94% yield).1H NMR (300 MHz, CDCl3) δ 6.24 (s, 1H), 5.00-5.03 (d, 1H).
References
[1] Patent: US2018/105527, 2018, A1. Location in patent: Paragraph 0553-0556
[2] Catalysis Letters, 2017, vol. 147, # 4, p. 837 - 844
BOC-DL-2-AMINOBUTYRIC ACID Preparation Products And Raw materials
Raw materials
Preparation Products
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