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Merck
CN

192198

Sigma-Aldrich

2,4,6-三异丙基苯磺酰基肼

90%

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别名:
2,4,6-三异丙基苯磺酰基肼, 2,4,6-三异丙基苯磺酰肼, TPSH
线性分子式:
[(CH3)2CH]3C6H2SO2NHNH2
CAS号:
分子量:
298.44
Beilstein:
2145001
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

90%

形式

powder

mp

110-112 °C (dec.) (lit.)

储存温度

−20°C

SMILES字符串

CC(C)c1cc(C(C)C)c(c(c1)C(C)C)S(=O)(=O)NN

InChI

1S/C15H26N2O2S/c1-9(2)12-7-13(10(3)4)15(20(18,19)17-16)14(8-12)11(5)6/h7-11,17H,16H2,1-6H3

InChI key

UGRVYFQFDZRNMQ-UHFFFAOYSA-N

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应用

2,4,6-Triisopropylbenzenesulfonyl hydrazide (TPSH) is a best source of diazene. It can be used as a selective reducing agent for the reduction of alkenes and other double bonds via in situ formation of diazene (diimide) in the presence of base. TPSH reduction method is efficiently used in the synthesis of polymers and natural products as it tolerates sensitive groups such as esters, ketones, or organometal complexes. It also undergoes condensation reaction with ketones and aldehydes to produce corresponding hydrazones that can be converted into reactive intermediates such as diazoalkanes, carbenes, carbenium ions, and alkyllithiums.
It can be used as a reagent to synthesize:
  • Nitrogen-containing polycyclic compounds by intramolecular cyclopropanation of N-alkyl indoles/pyrroles.
  • Vinyl sulfones by sulfonylation reaction of vinyl bromides.
  • Nitrile derivatives from carbonyl compounds via formation of corresponding hydrazones.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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The asymmetric synthesis of cyclopentane derivatives by palladium-catalyzed coupling of prochiral alkylboron compounds.
Cho SY and Shibasaki M.
Tetrahedron Asymmetry, 9(21), 3751-3754 (1998)
Synthesis and x-ray crystal structure of anti-dithia [3.3](2.6) triquinacenophane.
Roberts WP and Shoham G.
Tetrahedron Letters, 22(49), 4895-4898 (1981)
Cobalt (II) Porphyrin-Catalyzed Intramolecular Cyclopropanation of N-Alkyl Indoles/Pyrroles with Alkylcarbene: Efficient Synthesis of Polycyclic N-Heterocycles
Reddy AR, et al.
Angewandte Chemie (International ed. in English), 55(5), 1810-1815 (2016)
2,4,6-Triisopropylbenzenesulfonylhydrazide
Chamberlin AR, et al.
Encyclopedia of Reagents for Organic Synthesis, Second Edition null
2, 4, 6-Tri-isopropylbenzenesulphonyl hydrazide: A convenient source of di-imide
Cusack NJ, et al.
Tetrahedron, 32(17) (1976)

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