Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List Phenol, 2-tricyclo[3.3.1.13,7]dec-1-yl-

Phenol, 2-tricyclo[3.3.1.13,7]dec-1-yl- synthesis

8synthesis methods
-

Yield:29799-07-3 83% ,38614-06-1 17%

Reaction Conditions:

with molybdenum hexacarbonyl at 120; for 2 h;Sealed tube;regioselective reaction;

Steps:

Alkylation of aromatic compound with 1-bromoadamantane. General procedure.

General procedure: Into a pressure microreactor of stainless steel of capacity 17 mL or into a glass ampule of capacity 10 mL (the results of parallel runs differed insignificantly) was charged 1-3 mmol of catalyst [Mo(CO)6, MoO2(acac)2, Cr(CO)6,CoBr2, CuBr, CuBr2, W(CO)6], 100 mmol of 1-bromoadamantane, and 500 mmol of aromatic compound, the reactor was hermetically closed (the ampule was sealed) and heated at 110-130° for 1-3 h. On completing the reaction the reactor (ampule) was cooled to room temperature, opened, the reaction mixture was neutralized with NaHCO3 and filtered through a bed of Al2O3. The unreacted aromatic compound was distilled off, the residue was distilled in propanol).

References:

Khusnutdinov;Shchadneva;Khisamova [Russian Journal of Organic Chemistry,2015,vol. 51,# 11,p. 1545 - 1550][Zh. Org. Khim.,2015,vol. 51,# 11,p. 1576 - 1581,6]

1357000-33-9 Synthesis
2-(Adamantan-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1357000-33-9
6 suppliers
inquiry

Phenol, 2-tricyclo[3.3.1.13,7]dec-1-yl-

38614-06-1
9 suppliers
inquiry