N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide

Base Information

Chemical Name:N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide
CAS No.:1422953-22-7
Molecular Formula:C₂₇H₄₁NO₃
Molecular Weight:427.627
Hs Code.:

Synonyms:N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide

Suppliers and Price of N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide

There total 3 articles about N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide 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: 88.0%

: 1422953-21-6
N,N-diethyl-3-methoxy-5-(methoxymethoxy)-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide

: 1422953-22-7
N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide

Guidance literature:: With camphor-10-sulfonic acid; In methanol; at 25 ℃; for 12h; Inert atmosphere;
DOI:10.1055/s-0032-1317544

Reference yield:

: 1422953-19-2
4-bromo-3-methoxy-5-(methoxymethoxy)benzoic acid

: 1422953-22-7
N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 0 - 25 °C / Inert atmosphere

2: bis-triphenylphosphine-palladium(II) chloride; cesium fluoride / N,N-dimethyl-formamide / 36 h / 90 °C / Inert atmosphere

3: camphor-10-sulfonic acid / methanol / 12 h / 25 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; camphor-10-sulfonic acid; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; cesium fluoride; In methanol; N,N-dimethyl-formamide; 2: |Stille Cross Coupling;
DOI:10.1055/s-0032-1317544

Reference yield:

: 1422953-20-5
4-bromo-N,N-diethyl-3-methoxy-5-(methoxymethoxy)benzamide

: 1422953-22-7
N,N-diethyl-3-hydroxy-5-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: bis-triphenylphosphine-palladium(II) chloride; cesium fluoride / N,N-dimethyl-formamide / 36 h / 90 °C / Inert atmosphere

2: camphor-10-sulfonic acid / methanol / 12 h / 25 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; camphor-10-sulfonic acid; cesium fluoride; In methanol; N,N-dimethyl-formamide; 1: |Stille Cross Coupling;
DOI:10.1055/s-0032-1317544