(1R,8R,8aR)-8-Benzyloxymethoxy-2,5,5,8a-tetramethyl-1,5,6,7,8,8a-hexahydro-naphthalene-1-carboxylic acid ethyl ester

Base Information

• Chemical Name: (1R,8R,8aR)-8-Benzyloxymethoxy-2,5,5,8a-tetramethyl-1,5,6,7,8,8a-hexahydro-naphthalene-1-carboxylic acid ethyl ester
• CAS No.: 120666-89-9
• Molecular Formula: C₂₅H₃₄O₄
• Molecular Weight: 398.543

Synonyms:(1R,8R,8aR)-8-Benzyloxymethoxy-2,5,5,8a-tetramethyl-1,5,6,7,8,8a-hexahydro-naphthalene-1-carboxylic acid ethyl ester

Chemical Property of (1R,8R,8aR)-8-Benzyloxymethoxy-2,5,5,8a-tetramethyl-1,5,6,7,8,8a-hexahydro-naphthalene-1-carboxylic acid ethyl ester

Chemical Property:

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Technology Process of (1R,8R,8aR)-8-Benzyloxymethoxy-2,5,5,8a-tetramethyl-1,5,6,7,8,8a-hexahydro-naphthalene-1-carboxylic acid ethyl ester

There total 4 articles about (1R,8R,8aR)-8-Benzyloxymethoxy-2,5,5,8a-tetramethyl-1,5,6,7,8,8a-hexahydro-naphthalene-1-carboxylic acid ethyl 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: 70.0%

(2E,4E)-5-(3-Benzyloxymethoxy-2,6,6-trimethyl-cyclohex-1-enyl)-3-methyl-penta-2,4-dienoic acid ethyl ester → (1R,8R,8aR)-8-Benzyloxymethoxy-2,5,5,8a-tetramethyl-1,5,6,7,8,8a-hexahydro-naphthalene-1-carboxylic acid ethyl ester (120666-89-9)

Guidance literature:

With N,N-dimethyl-aniline; at 240 ℃;

DOI:10.1021/jo00272a005

Reference yield:

Benzyloxymethyl chloride (3587-60-8) → (1R,8R,8aR)-8-Benzyloxymethoxy-2,5,5,8a-tetramethyl-1,5,6,7,8,8a-hexahydro-naphthalene-1-carboxylic acid ethyl ester (120666-89-9)

Guidance literature:

Multi-step reaction with 3 steps

1: iPr₂NEt / CH₂Cl₂

2: NaH / tetrahydrofuran / Heating

3: 70 percent / N,N-dimethylaniline / 240 °C

With sodium hydride; N,N-dimethyl-aniline; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1021/jo00272a005

Reference yield:

4-(3-hydroxy-2,6,6-trimethylcyclohex-1-enyl)but-3-en-2-one (14398-34-6) → (1R,8R,8aR)-8-Benzyloxymethoxy-2,5,5,8a-tetramethyl-1,5,6,7,8,8a-hexahydro-naphthalene-1-carboxylic acid ethyl ester (120666-89-9)

Guidance literature:

Multi-step reaction with 3 steps

1: iPr₂NEt / CH₂Cl₂

2: NaH / tetrahydrofuran / Heating

3: 70 percent / N,N-dimethylaniline / 240 °C

With sodium hydride; N,N-dimethyl-aniline; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1021/jo00272a005

upstream raw materials:

Benzyloxymethyl chloride

4-(3-hydroxy-2,6,6-trimethylcyclohex-1-enyl)but-3-en-2-one

(E)-4-(3-Benzyloxymethoxy-2,6,6-trimethyl-cyclohex-1-enyl)-but-3-en-2-one

Downstream raw materials:

(1R,5R,6S,7R)-5-Benzyloxymethoxy-2,2,6-trimethyl-8-methylene-11-oxa-tricyclo[5.3.2.0^1,6]dodec-9-ene

(1R,5R,6S,7R,8R)-5-Benzyloxymethoxy-2,2,6,8-tetramethyl-11-oxa-tricyclo[5.3.2.0^1,6]dodecan-10-one

(1R,5R,6S,7R,8R)-5-Benzyloxymethoxy-2,2,6,8-tetramethyl-11-oxa-tricyclo[5.3.2.0^1,6]dodec-9-en-8-ol

(4S,4aS,5S,8aR)-5-Benzyloxymethoxy-4-hydroxymethyl-3,4a,8,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-4H-naphthalen-1-one

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