4-Nitro-benzoic acid (E)-(R)-1-methyl-3-((1R,5S)-2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl ester

Base Information

Chemical Name:4-Nitro-benzoic acid (E)-(R)-1-methyl-3-((1R,5S)-2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl ester
CAS No.:307500-74-9
Molecular Formula:C₂₁H₂₇NO₄
Molecular Weight:357.45
Hs Code.:

Synonyms:4-Nitro-benzoic acid (E)-(R)-1-methyl-3-((1R,5S)-2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl ester

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Chemical Property of 4-Nitro-benzoic acid (E)-(R)-1-methyl-3-((1R,5S)-2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl ester

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Technology Process of 4-Nitro-benzoic acid (E)-(R)-1-methyl-3-((1R,5S)-2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl ester

There total 5 articles about 4-Nitro-benzoic acid (E)-(R)-1-methyl-3-((1R,5S)-2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl 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:

: 202481-73-0,54082-69-8
4-(2,5,6,6-tetramethyl-2-cyclohexen-1-yl)-3-buten-2-one

: 307500-74-9
4-Nitro-benzoic acid (E)-(R)-1-methyl-3-((1R,5S)-2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / NaBH₄ / CH₂Cl₂; methanol / 0 °C

2: 60.2 percent Chromat_. / porcine pancreatic lipase / various solvent(s) / 24 h / 20 °C

3: KOH / methanol

4: pyridine / CH₂Cl₂

With pyridine; potassium hydroxide; sodium tetrahydroborate; porcine pancreatic lipase; In methanol; dichloromethane; 1: Reduction / 2: Acetylation / 3: Saponification / 4: Acylation;
DOI:10.1002/1099-0690(200009)2000:17<3031::AID-EJOC3031>3.0.CO;2-7

Reference yield:

: 564-76-1,70223-18-6
α-irol

: 307500-74-9
4-Nitro-benzoic acid (E)-(R)-1-methyl-3-((1R,5S)-2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 60.2 percent Chromat_. / porcine pancreatic lipase / various solvent(s) / 24 h / 20 °C

2: KOH / methanol

3: pyridine / CH₂Cl₂

With pyridine; potassium hydroxide; porcine pancreatic lipase; In methanol; dichloromethane; 1: Acetylation / 2: Saponification / 3: Acylation;
DOI:10.1002/1099-0690(200009)2000:17<3031::AID-EJOC3031>3.0.CO;2-7

Reference yield:

: Acetic acid (E)-1-methyl-3-(2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl ester

: 307500-74-9
4-Nitro-benzoic acid (E)-(R)-1-methyl-3-((1R,5S)-2,5,6,6-tetramethyl-cyclohex-2-enyl)-allyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: KOH / methanol

2: 60.2 percent Chromat_. / porcine pancreatic lipase / various solvent(s) / 24 h / 20 °C

3: KOH / methanol

4: pyridine / CH₂Cl₂

With pyridine; potassium hydroxide; porcine pancreatic lipase; In methanol; dichloromethane; 1: Saponification / 2: Acetylation / 3: Saponification / 4: Acylation;
DOI:10.1002/1099-0690(200009)2000:17<3031::AID-EJOC3031>3.0.CO;2-7