tert-butyl [(R)-2-(2-acetyl-4-bromophenoxy)-1-methylethyl]carbamate

Base Information

• Chemical Name: tert-butyl [(R)-2-(2-acetyl-4-bromophenoxy)-1-methylethyl]carbamate
• CAS No.: 1345731-83-0
• Molecular Formula: C₁₆H₂₂BrNO₄
• Molecular Weight: 372.259
• Mol file: 1345731-83-0.mol

Synonyms:tert-butyl [(R)-2-(2-acetyl-4-bromophenoxy)-1-methylethyl]carbamate

Chemical Property of tert-butyl [(R)-2-(2-acetyl-4-bromophenoxy)-1-methylethyl]carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of tert-butyl [(R)-2-(2-acetyl-4-bromophenoxy)-1-methylethyl]carbamate

There total 1 articles about tert-butyl [(R)-2-(2-acetyl-4-bromophenoxy)-1-methylethyl]carbamate 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: 52.0%

5-Bromo-2-hydroxyacetophenone (1450-75-5) + (R)-2-tertbutoxycarbonylamino-1-propanol (79069-13-9,127516-56-7,147252-84-4,106391-86-0) → tert-butyl [(R)-2-(2-acetyl-4-bromophenoxy)-1-methylethyl]carbamate (1345731-83-0)

Guidance literature:

With triphenylphosphine; diethylazodicarboxylate; In toluene; at 20 ℃; for 4h;

DOI:10.1016/j.bmcl.2011.08.093

Reference yield:

tert-butyl [(R)-2-(2-acetyl-4-bromophenoxy)-1-methylethyl]carbamate (1345731-83-0) → (3R,5S)-7-bromo-4-(4-chlorobenzoyl)-3,5-dimethyl-2,3,4,5-tetrahydro-1,4-benzoxazepine (1345731-56-7)

Guidance literature:

Multi-step reaction with 3 steps

1: trifluoroacetic acid / dichloromethane / 4 h / 20 °C

2: sodium tetrahydroborate / ethanol / 0 - 20 °C

3: sodium hydroxide / tetrahydrofuran / 1 h / 20 °C

With sodium tetrahydroborate; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; ethanol; dichloromethane;

DOI:10.1016/j.bmcl.2011.08.093

Reference yield:

tert-butyl [(R)-2-(2-acetyl-4-bromophenoxy)-1-methylethyl]carbamate (1345731-83-0) → (3R,5S)-4-(4-chlorobenzoyl)-3,5-dimethyl-2,3,4,5-tetrahydro-1,4-benzoxazepine-7-carbonitrile (1345731-52-3)

Guidance literature:

Multi-step reaction with 4 steps

1: trifluoroacetic acid / dichloromethane / 4 h / 20 °C

2: sodium tetrahydroborate / ethanol / 0 - 20 °C

3: sodium hydroxide / tetrahydrofuran / 1 h / 20 °C

4: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

With sodium tetrahydroborate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2011.08.093

upstream raw materials:

5-Bromo-2-hydroxyacetophenone

(R)-2-tertbutoxycarbonylamino-1-propanol

Downstream raw materials:

(3R,5S)-7-bromo-4-(4-chlorobenzoyl)-3,5-dimethyl-2,3,4,5-tetrahydro-1,4-benzoxazepine

(3R,5S)-4-(4-chlorobenzoyl)-3,5-dimethyl-2,3,4,5-tetrahydro-1,4-benzoxazepine-7-carbonitrile