6-BROMO-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER

Base Information

• Chemical Name: 6-BROMO-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER
• CAS No.: 893566-74-0
• Molecular Formula: C14H18BrNO2
• Molecular Weight: 312.206
• Mol file: 893566-74-0.mol

Synonyms:6-bromo-3,4-dihydro-1H-isoquinoline-2-carboxylicacid tert-butyl ester;tert-Butyl6-bromo-3,4-dihydroisoquinoline-2(1H)-carboxylate;

Chemical Property of 6-BROMO-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER

Chemical Property:

• Vapor Pressure: 8.48E-06mmHg at 25°C
• Refractive Index: 1.559
• Boiling Point: 374.2 °C at 760 mmHg
• PKA: -1.56±0.20(Predicted)
• Flash Point: 180.1 °C
• PSA: 29.54000
• Density: 1.353g/cm³
• LogP: 3.68020
• Storage Temp.: 2-8°C

Purity/Quality:

97% ^*data from raw suppliers

2-Boc-6-bromo-3,4-dihydro-1H-isoquinoline ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 6-BROMO-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER

There total 12 articles about 6-BROMO-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: 100.0%

6-bromo-1,2,3,4-tetrahydroisoquinoline (226942-29-6) + di-tert-butyl dicarbonate (24424-99-5) → 6-bromo-2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline (893566-74-0)

Guidance literature:

In tetrahydrofuran; at 10 - 35 ℃; for 15h;

Reference yield: 98.6%

→ 6-bromo-2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline (893566-74-0)

Guidance literature:

With triethylamine; In tetrahydrofuran; at 20 ℃; for 5h;

Reference yield: 97.0%

6-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride (215798-19-9) + di-tert-butyl dicarbonate (24424-99-5) → 6-bromo-2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline (893566-74-0)

Guidance literature:

With triethylamine; In methanol; at 20 ℃; for 20h; Inert atmosphere;

upstream raw materials:

6-bromo-1,2,3,4-tetrahydroisoquinoline

di-tert-butyl dicarbonate

8-bromo-1,2,3,4-tetrahydroisoquinoline

tert-butyl 6-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate

Downstream raw materials:

6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

tert-butyl 8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

2-[(1-methylethyl)oxy]-5-[5-(1,2,3,4-tetrahydro-6-isoquinolinyl)-1,3,4-thiadiazol-2-yl]benzonitrile

1,1-dimethylethyl 6-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,3,4-thiadiazol-2-yl)-3,4-dihydro-2(1H)-isoquinolinecarboxylate