31039-85-7

Upstream product

• 1460-02-2 1,3,5-Tri-tert-butylbenzene 
• 3975-77-7 1-bromo-2,4,6-tri-tert-butylbenzene 
• 1634-04-4 tert-butyl methyl ether 
• 1618100-32-5 diethyl 1-(2',4',6'-tri-tert-butylphenyl)vinyl phosphate 
• 124-38-9 carbon dioxide 
• 20208-55-3 2,4,6-tri-tert-butylbenzoyl chloride 
• 66415-27-8 2,4,6-tri-tert-butylbenzoic acid 
• 31039-83-5 Aethyl-2.4.6-tri-tert.butylphenylpropiolat 
• 31039-82-4 2-iodo-1,3,5-tri-tert-butylbenzene 
• 31039-84-6 3-(2',4',6'-tri-tert-butylphenyl)propiolic acid 
• 100938-86-1 2-(2,4,6-tri-tert-butylphenyl)phosphaacetylene 
• 19513-48-5 Dichlorocarbene 

Downstream Products

• 135394-35-3 3-(2,4,6-Tri-tert-butylphenyl)propindithiosaeure-methylester 
• 31039-86-8 2.4.6,2'.4'.6'-Hexa-tert.-butyldiphenylacetylen 
• 460710-68-3 C₂₄H₄₁N₂P 
• 1182842-83-6 C₄₃H₇₂P₂ 
• 612851-91-9 1-tert-butyl-3-methyl-2,4-bis(2,4,6-tri-tert-butylphenyl)-1,3-diphosphacyclobutane-2,4-diyl 
• 1618100-13-2 1-bromo-1-(2',4',6'-tri-tert-butylphenyl)ethene 
• 1618100-14-3 (E)-[2-D]-1-bromo-1-(2',4',6'-tri-tert-butylphenyl)ethene 
• 1628708-89-3 (Z)-[2-D]-1-bromo-1-(2',4',6'-tri-tert-butylphenyl)ethene 
• 33241-82-6 2',4',6'-tri-tert-butylstyrene 
• 1618100-19-8 [1-(2',4',6'-tri-tert-butylphenyl)vinyl](trimethyl)-stannane 
• 1618099-90-3 [2-D]-1-(2,4,6-tri-tert-butylphenyl)acetylene 

Relevant academic research and scientific papers

Highly syn selective addition of aqueous HBr to hydrophobically shielded arylalkynes

Hydrophobically shielded alkynes HC≡C-aryl, carrying 2,6-di- and 2,4,6-tri-tert-butylphenyl as the aryl group, can add aqueous HBr on heating in moist chloroform solutions to produce pure H2C=C(-Br)-aryl (isolated yields 96%, no hydrolysis). Em

Highly syn selective addition of aqueous HBr to hydrophobically shielded arylalkynes

Hydrophobically shielded alkynes HCC-aryl, carrying 2,6-di- and 2,4,6-tri-tert-butylphenyl as the aryl group, can add aqueous HBr on heating in moist chloroform solutions to produce pure H2CC(-Br)-aryl (isolated yields 96%, no hydrolysis). Employment of DCC-aryl furnished initially only the E stereoisomer of DHCC(-Br)-aryl (stereospecific syn addition), which was slowly both dedeuteriated and partially transformed to the Z stereoisomer by HBr. The strongly retarded HBr addition to H3C-CC-aryl in moist chloroform produced again more E than Z product, whereas a thermodynamic E/Z ratio of 10:87 was found in moist acetic acid. Substitution of Br by LiSnMe3produced H2CC(-SnMe3)-aryl with well resolved long range 119Sn NMR coupling constants.