Production Method 1

158732-35-5

87172-82-5

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Methanol ;  rt

Reference

Metal-induced chiral folding of depsipeptide dendrimers

Buschhaus, Boris; et al, Chemistry - A European Journal, 2005, 11(12), 3530-3540

Production Method 2

2743-38-6

87172-82-5

Reaction Conditions

1.1 Solvents: Water ;  4 h, 97 °C; 97 °C → 15 °C; 1 h, 12 - 15 °C

Reference

Process of preparing O-acyltartaric acids

, Poland, , ,

Production Method 3

87-69-4

87172-82-5

Reaction Conditions

Reference

Tartaric acid and its O-acyl derivatives. Part 14: Nucleophilic ring-opening reaction of nonsymmetrically substituted tartaric acid anhydride as a tool for the synthesis of totally differentiated tartaric acid derivatives

Bernas, Urszula; et al, Tetrahedron, 2015, 71(23), 4047-4052

Production Method 4

87-69-4

98-88-4

87172-82-5

64339-95-3

100675-53-4

2743-38-6

Reaction Conditions

1.1 Solvents: 1,2-Dimethoxyethane ;  4 h, reflux

Reference

Tartaric acid and its acyl derivatives. Part 5. Direct synthesis of monoacyltartaric acids and novel mono(benzoyl)tartaric anhydride: unusual findings in tartaric acid acylation

Bernas, Urszula; et al, ARKIVOC (Gainesville, 2010, (11), 1-12

(2R,3R)-2-(Benzoyloxy)-3-hydroxysuccinic acid Raw materials

• L(+)-Tartaric acid
• Di-O-benzoyl L-Tartaric Acid
• Benzoyl chloride
• Butanedioic acid, 2-(benzoyloxy)-3-hydroxy-, 1,4-bis(phenylmethyl) ester, (2R,3R)-

(2R,3R)-2-(Benzoyloxy)-3-hydroxysuccinic acid Preparation Products

• (3R,4R)-2,5-dioxotetrahydrofuran-3,4-diyl Dibenzoate (64339-95-3)
• (100675-53-4)
• Di-O-benzoyl L-Tartaric Acid (2743-38-6)
• (2R,3R)-2-(Benzoyloxy)-3-hydroxysuccinic acid (87172-82-5)

• 1. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?
  Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
• 2. Emulsion soft templating of carbide-derived carbon nanospheres with controllable porosity for capacitive electrochemical energy storage?
  M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
• 3. Empowering microfluidics by micro-3D printing and solution-based mineral coating?
  Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
• 4. Fast synthesis of red Li3BaSrLn3(WO4)8:Eu3+ phosphors for white LEDs under near-UV excitation by a microwave-assisted solid state reaction method and photoluminescence studies
  Bo Wei,Zhenyu Liu,Chen Xie,Shu Yang,Wentao Tang,Aiwei Gu,Wing-Tak Wong,Ka-Leung Wong J. Mater. Chem. C, 2015,3, 12322-12327
• 5. Enabling non-flammable Li-metal batteries via electrolyte functionalization and interface engineering?
  Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acid esters
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acids and derivatives Benzoic acid esters

• 62708-56-9((-)-Dibenzoyl-L-tartaric acid monohydrate)
• 71607-31-3(Di-p-toluoyl-D-tartaric Acid Monohydrate)
• 71607-32-4((2S,3S)-2,3-Bis((4-methylbenzoyl)oxy)succinic acid hydrate)
• 80822-15-7((+)-Dibenzoyl-D-Tartaric Acid Monohydrate)
• 918447-59-3(Butanedioic acid, 2,3-bis[(4-methylbenzoyl)oxy]-, (2R,3R)-, compd. withethyl acetate (1:1))
• 4202-11-3(dipropyl 2,3-bis(benzoyloxy)butanedioate)
• 32634-68-7((+)-O,O’-Di-p-toluoyl-D-tartaric Acid)
• 32634-66-5((-)-Di-p-toluoyl-L-tartaric Acid)
• 2743-38-6(Di-O-benzoyl L-Tartaric Acid)
• 217968-14-4(Butanedioic acid,2,3-bis[(4-methylbenzoyl)oxy]-, ion(2-), (2S,3S)-)