(Z)-4-(chlorophenylmethylene)-10,10-dimethyl-2-tosyl-2-azaspiro[4.6]undec-7-ene

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Chemical Name:(Z)-4-(chlorophenylmethylene)-10,10-dimethyl-2-tosyl-2-azaspiro[4.6]undec-7-ene
CAS No.:1404440-17-0
Molecular Formula:C₂₆H₃₀ClNO₂S
Molecular Weight:456.049
Hs Code.:

Synonyms:(Z)-4-(chlorophenylmethylene)-10,10-dimethyl-2-tosyl-2-azaspiro[4.6]undec-7-ene

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Chemical Property of (Z)-4-(chlorophenylmethylene)-10,10-dimethyl-2-tosyl-2-azaspiro[4.6]undec-7-ene

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Technology Process of (Z)-4-(chlorophenylmethylene)-10,10-dimethyl-2-tosyl-2-azaspiro[4.6]undec-7-ene

There total 7 articles about (Z)-4-(chlorophenylmethylene)-10,10-dimethyl-2-tosyl-2-azaspiro[4.6]undec-7-ene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

: (±)-N-(((1R,5R,6S)-5-hydroxy-3,3-dimethylbicyclo[4.1.0]heptan-1-yl)methyl)-4-methyl-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

: 1404440-17-0
(Z)-4-(chlorophenylmethylene)-10,10-dimethyl-2-tosyl-2-azaspiro[4.6]undec-7-ene

Guidance literature:: With iron(III) chloride; In dichloromethane; at -15 ℃; for 0.05h;
DOI:10.1021/jo301764g

Reference yield:

: 15466-96-3
3-isobutoxy-5,5-dimethylcyclohex-2-en-1-one

: 1404440-17-0
(Z)-4-(chlorophenylmethylene)-10,10-dimethyl-2-tosyl-2-azaspiro[4.6]undec-7-ene

Guidance literature:: Multi-step reaction with 6 steps

1.1: N,N,N,N,-tetramethylethylenediamine; n-butyllithium / 4 h / 20 °C

1.2: 2 h / -78 - 20 °C

2.1: methyl iodide / dichloromethane / 72 h / 45 °C

3.1: potassium carbonate / acetone / 10 h / 20 °C

4.1: cerium(III) chloride heptahydrate; sodium tetrahydroborate / methanol / 1 h / 0 °C

5.1: diethylzinc / dichloromethane; diethyl ether / 10 h / 0 - 30 °C

6.1: iron(III) chloride / dichloromethane / 0.05 h / -15 °C

With iron(III) chloride; sodium tetrahydroborate; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; cerium(III) chloride heptahydrate; diethylzinc; potassium carbonate; methyl iodide; In methanol; diethyl ether; dichloromethane; acetone;
DOI:10.1021/jo301764g

Reference yield:

: 126-81-8
dimedone

: 1404440-17-0
(Z)-4-(chlorophenylmethylene)-10,10-dimethyl-2-tosyl-2-azaspiro[4.6]undec-7-ene

Guidance literature:: Multi-step reaction with 7 steps

1.1: toluene-4-sulfonic acid / toluene / Dean-Stark; Reflux

2.1: N,N,N,N,-tetramethylethylenediamine; n-butyllithium / 4 h / 20 °C

2.2: 2 h / -78 - 20 °C

3.1: methyl iodide / dichloromethane / 72 h / 45 °C

4.1: potassium carbonate / acetone / 10 h / 20 °C

5.1: cerium(III) chloride heptahydrate; sodium tetrahydroborate / methanol / 1 h / 0 °C

6.1: diethylzinc / dichloromethane; diethyl ether / 10 h / 0 - 30 °C

7.1: iron(III) chloride / dichloromethane / 0.05 h / -15 °C

With iron(III) chloride; sodium tetrahydroborate; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; cerium(III) chloride heptahydrate; diethylzinc; potassium carbonate; toluene-4-sulfonic acid; methyl iodide; In methanol; diethyl ether; dichloromethane; acetone; toluene;
DOI:10.1021/jo301764g