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Merck
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Key Documents

193801

Sigma-Aldrich

4,4′-Di-tert-butylbiphenyl

99%

동의어(들):

1-tert-Butyl-4-(4-tert-butylphenyl)benzene, 4,4′-Bis(1,1-dimethylethyl)-1,1′-biphenyl, 4,4′-Di-tert-butyl-1,1′-biphenyl, DBB, p,p′-Di-tert-butylbiphenyl

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About This Item

Linear Formula:
(CH3)3CC6H4C6H4C(CH3)3
CAS Number:
Molecular Weight:
266.42
Beilstein:
2095855
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

99%

형태

solid

bp

190-192 °C/13 mmHg (lit.)

mp

126-130 °C (lit.)

SMILES string

CC(C)(C)c1ccc(cc1)-c2ccc(cc2)C(C)(C)C

InChI

1S/C20H26/c1-19(2,3)17-11-7-15(8-12-17)16-9-13-18(14-10-16)20(4,5)6/h7-14H,1-6H3

InChI key

CDKCEZNPAYWORX-UHFFFAOYSA-N

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일반 설명

4,4′-Di-tert-butylbiphenyl along with lithium catalyzes:
  • reaction of chloromethyl ethyl ether and different carbonyl compounds to yield corresponding hydroxyethers
  • reductive opening of N-phenylazetidine

애플리케이션

4,4′-Di-tert-butylbiphenyl was used in production of homoallylic amine derivatives. It was also used in the preparation of lithium di-tert-butylbiphenylide, a radical anion, superior to sodium or lithium naphthalenides for metalation reactions.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

C E Neipp et al.
The Journal of organic chemistry, 66(2), 531-537 (2001-06-30)
Lithiation of the N-2,4,6-triisopropylbenzenesulfonyl-2-pyrroline (16) and treatment of the resulting cyclic vinyllithium reagent with R2CuCNLi2 produced an acyclic vinyl organometallic species that, when treated with an electrophile (H2O or RX), gave the homoallylic sulfonamides 18a-k in 37-93% yields and in
4, 4'-Di -tert -butylbiphenyl-catalysed reductive opening of azetidines with lithium: A direct preparation of 3, N-dilithioalkylamines.
Almena J, et al.
Tetrahedron, 50(19), 5775-5782 (1994)
The Journal of Organic Chemistry, 55, 1528-1528 (1990)
4, 4′-Di-tert-butylbiphenyl-catalysed lithiation of chloromethyl ethyl ether: A barbier-type new and easy alternative to ethyl lithiomethyl ether.
Guijarro A and Yus M.
Tetrahedron Letters, 34(21), 3487-3490 (1993)

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