2-[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-pent-4-enoic acid cyclohexyl ester

Base Information

Chemical Name:2-[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-pent-4-enoic acid cyclohexyl ester
CAS No.:125443-73-4
Molecular Formula:C₂₁H₃₃NO₂
Molecular Weight:331.499
Hs Code.:

Synonyms:2-[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-pent-4-enoic acid cyclohexyl ester

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Chemical Property of 2-[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-pent-4-enoic acid cyclohexyl ester

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Technology Process of 2-[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-pent-4-enoic acid cyclohexyl ester

There total 3 articles about 2-[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-pent-4-enoic acid cyclohexyl 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: 85.0%

: 125423-97-4
[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-acetic acid cyclohexyl ester

: 106-95-6
allyl bromide

: 125443-73-4
2-[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-pent-4-enoic acid cyclohexyl ester

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 - -50 ℃; for 5h;

Reference yield:

: 464-49-3,68546-28-1
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

: 125443-73-4
2-[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-pent-4-enoic acid cyclohexyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / BF₃*Et₂O / toluene / 36 h / Heating

2: 85 percent / LDA / tetrahydrofuran / 5 h / -78 - -50 °C

With boron trifluoride diethyl etherate; lithium diisopropyl amide; In tetrahydrofuran; toluene;

Reference yield:

: 55636-84-5
glycine cyclohexyl ester

: 125443-73-4
2-[(1R,4R)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-(2E)-ylideneamino]-pent-4-enoic acid cyclohexyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / BF₃*Et₂O / toluene / 36 h / Heating

2: 85 percent / LDA / tetrahydrofuran / 5 h / -78 - -50 °C

With boron trifluoride diethyl etherate; lithium diisopropyl amide; In tetrahydrofuran; toluene;