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Boc-D-Pro-OMe

Boc-D-Pro-OMe Suppliers list
Company Name: Shanghai Chiral Chemicals Inc.  Gold
Tel: 021-37285021 13472570865
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Company Name: Shandong Lonyuta Pharmaceutical Technology Co., Ltd  Gold
Tel: 0534-2152677 17862520650
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Company Name: J & K SCIENTIFIC LTD.  
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Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
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Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com

Boc-D-Pro-OMe manufacturers

  • BOC-D-PRO-OME
  • BOC-D-PRO-OME pictures
  • $1.00
  • 2019-12-20
  • CAS:73323-65-6
  • Min. Order: 1KG
  • Purity: 99%
Boc-D-Pro-OMe Basic information
Product Name:Boc-D-Pro-OMe
Synonyms:BOC-D-PROLINE METHYL ESTER;BOC-D-PYRD(2)-OME;R-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID METHYL ESTER;N-ALPHA-T-BUTOXYCARBONYL-D-PROLINE METHYL ESTER;N-ALPHA-T-BUTOXYCARBONYL-D-PYRROLIDINE-2-CARBOXYLIC ACID METHYL ESTER;N-tert-Butoxycarbonyl-D-Proline methyl ester;BOC-D-PROLINE METHYLESTER LIQUID;N-BOC-D-PROLINE METHYL ESTER
CAS:73323-65-6
MF:C11H19NO4
MW:229.27
EINECS:233-720-0
Product Categories:Pyrrole&Pyrrolidine&Pyrroline
Mol File:73323-65-6.mol
Boc-D-Pro-OMe Structure
Boc-D-Pro-OMe Chemical Properties
Boiling point 288.6±33.0 °C(Predicted)
density 1.120±0.06 g/cm3(Predicted)
refractive index 1.4510-1.4550
storage temp. Sealed in dry,2-8°C
solubility Soluble in DMSO.
pka-3.35±0.40(Predicted)
form Oil
color Clear Colourless
Optical Rotation59.8°(C=0.01g/ml MEOH)
InChIInChI=1S/C11H19NO4/c1-11(2,3)16-10(14)12-7-5-6-8(12)9(13)15-4/h8H,5-7H2,1-4H3/t8-/m1/s1
InChIKeyWVDGSSCWFMSRHN-MRVPVSSYSA-N
SMILESN1(C(OC(C)(C)C)=O)CCC[C@@H]1C(OC)=O
CAS DataBase Reference73323-65-6(CAS DataBase Reference)
Safety Information
HazardClass IRRITANT
HS Code 2933998090
MSDS Information
Boc-D-Pro-OMe Usage And Synthesis
UsesN-Boc-D-proline methyl ester is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Synthesis
N-Boc-D-proline

37784-17-1

Iodomethane

74-88-4

BOC-D-PRO-OME

73323-65-6

To a mixture of (R)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid (5.8 g, 27 mmol) and potassium carbonate (8.6 g, 62 mmol) in tetrahydrofuran (160 mL) was added iodomethane (4.0 mL, 65 mmol). The reaction mixture was heated to reflux for 17 hours and subsequently cooled to room temperature. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The crude product was purified by automated column chromatography using petroleum ether/ethyl acetate (3:1, v/v) as eluent to afford (R)-1-tert-butyl 2-methyl pyrrolidine-1,2-dicarboxylate (6.0 g, 65% yield) as a yellow oil.

References[1] Patent: WO2013/131018, 2013, A1. Location in patent: Page/Page column 38
Tag:Boc-D-Pro-OMe(73323-65-6) Related Product Information
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