6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Base Information

Chemical Name:6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester
CAS No.:164148-88-3
Molecular Formula:C₂₁H₂₅NO₃
Molecular Weight:339.434
Hs Code.:

Synonyms:6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Suppliers and Price of 6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl 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 6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

There total 6 articles about 6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl 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: 99.2%

: 100-39-0
benzyl bromide

: 158984-83-9
N-tert-butoxycarbonyl-6-hydroxy-1,2,3,4-tetrahydroisoquinoline

: 164148-88-3
6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 12h;

Reference yield:

: 591-31-1
3-methoxy-benzaldehyde

: 164148-88-3
6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: ammonium acetate; acetic acid / 12 h / 100 °C

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 12 h / 0 - 80 °C

3.1: hydrogenchloride / water / 1 h / 60 °C

4.1: hydrogenchloride / isopropyl alcohol; water / 18 h / 20 °C

5.1: hydrogen bromide; water / 5 h / Reflux

6.1: triethylamine / tetrahydrofuran; water

7.1: sodium hydride / mineral oil; N,N-dimethyl-formamide / 1 h / 0 - 20 °C

7.2: 1 h

With hydrogenchloride; lithium aluminium tetrahydride; ammonium acetate; water; hydrogen bromide; sodium hydride; acetic acid; triethylamine; In tetrahydrofuran; water; N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;
DOI:10.1021/jm3014103

Reference yield:

: 2039-67-0
2-(3-methoxyphenyl)-1-ethanamine

: 164148-88-3
6-benzyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / water / 1 h / 60 °C

2.1: hydrogenchloride / isopropyl alcohol; water / 18 h / 20 °C

3.1: hydrogen bromide; water / 5 h / Reflux

4.1: triethylamine / tetrahydrofuran; water

5.1: sodium hydride / mineral oil; N,N-dimethyl-formamide / 1 h / 0 - 20 °C

5.2: 1 h

With hydrogenchloride; water; hydrogen bromide; sodium hydride; triethylamine; In tetrahydrofuran; water; N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;
DOI:10.1021/jm3014103