产品名称
三苯基氯甲烷, 97%
InChI
1S/C19H15Cl/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
InChI key
JBWKIWSBJXDJDT-UHFFFAOYSA-N
SMILES string
ClC(c1ccccc1)(c2ccccc2)c3ccccc3
assay
97%
bp
230-235 °C/20 mmHg (lit.)
mp
109-112 °C (lit.)
Quality Level
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Application
三苯甲基氯可用作以下应有的催化剂:
- Ritter型合成,通过萘酚,芳基醛和乙腈进行一锅三组分反应,合成1-氨基烷基-2-萘酚。
- 通过偶苯酰与醛、伯胺以及乙酸铵进行一锅多组分反应,合成1,2,4,5-四取代咪唑。
- 在无溶剂条件下通过酚、芳香醛和酰胺进行一锅多组分反应制备酰胺烷基酚。
- 通过芳香醛、胺和β-酮酯进行一锅多组分反应合成取代哌啶。
胺、醇和硫醇的保护剂。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
One pot synthesis of 1, 2, 4, 5-tetrasubstituted-imidazoles catalyzed by trityl chloride in neutral media
Moosavi-Zare AR, et al.
Royal Society of Chemistry Advances, 4(105), 60636-60639 (2014)
Tetrahedron Letters, 48, 5017-5017 (2007)
Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature
Khazaei A, et al.
Applied Catalysis A: General, 386(1-2), 179-187 (2010)
Trityl chloride as an efficient organic catalyst for one-pot, five-component and diastereoselective synthesis of highly substituted piperidines
Sajadikhah SS, et al.
Research on Chemical Intermediates, 40(2), 723-736 (2014)
Greene, T.W. Wuts, P.G.M.
Protective Groups in Organic Synthesis (1991)
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