(1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester

Base Information

Chemical Name:(1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester
CAS No.:74725-38-5
Molecular Formula:C₂₃H₂₂Cl₂O₄
Molecular Weight:433.331
Hs Code.:

Synonyms:(1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester

Suppliers and Price of (1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester

There total 1 articles about (1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester 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%

: 67-66-3,8013-54-5
chloroform

: 74725-37-4
(+/-)-3c,6c-diphenyl-cyclohex-4-ene-1r,2t-dicarboxylic acid dimethyl ester

: 74725-38-5
(1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester

Guidance literature:: With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; 1.) 0 deg C, 2 h; 2.) room temp., 14 h;
DOI:10.1021/jo01309a024

Reference yield: 58.0%

: 74725-38-5
(1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester

: 74725-39-6
((1R,2S,3S,4S,5R,6S)-7,7-Dichloro-4-hydroxymethyl-2,5-diphenyl-bicyclo[4.1.0]hept-3-yl)-methanol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; for 14h; Ambient temperature;
DOI:10.1021/jo01309a024

Reference yield:

: 74725-38-5
(1R,2S,3S,4S,5R,6S)-7,7-Dichloro-2,5-diphenyl-bicyclo[4.1.0]heptane-3,4-dicarboxylic acid dimethyl ester

: 74725-56-7
(1aR,2S,9R,9aS)-1,1-Dichloro-2,9-diphenyl-1a,2,3,8,9,9a-hexahydro-1H-cyclopropa[b]anthracene

Guidance literature:: Multi-step reaction with 5 steps

1: 58 percent / LiAlH₄ / tetrahydrofuran / 14 h / Ambient temperature

2: 80 percent / Et₃N / CH₂Cl₂ / 1 h / Ambient temperature

3: 59 percent / NaI / acetone / 8 h / Heating

4: 88 percent / KO-t-Bu / tetrahydrofuran / 0.5 h

5: 80 percent / CH₂Cl₂ / 2 h / Heating

With lithium aluminium tetrahydride; potassium tert-butylate; triethylamine; sodium iodide; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1021/jo01309a024