1-BENZYL-OCTAHYDRO-PYRROLO[3,4-B]PYRROLE

Base Information

• Chemical Name: 1-BENZYL-OCTAHYDRO-PYRROLO[3,4-B]PYRROLE
• CAS No.: 132414-50-7
• Molecular Formula: C13H18N2
• Molecular Weight: 202.299
• Hs Code.: 2933990090
• Mol file: 132414-50-7.mol

Synonyms:1-BENZYL-OCTAHYDRO-PYRROLO[3,4-B]PYRROLE;1-Benzylhexahydropyrrolo[3,4-b]pyrrole

Chemical Property of 1-BENZYL-OCTAHYDRO-PYRROLO[3,4-B]PYRROLE

Chemical Property:

• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.57
• Boiling Point: 304.35 °C at 760 mmHg
• PKA: 10.80±0.20(Predicted)
• Flash Point: 127.717 °C
• PSA: 15.27000
• Density: 1.074 g/cm³
• LogP: 1.74700
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C

Purity/Quality:

97% ^*data from raw suppliers

1-Benzyloctahydropyrrolo[3,4-b]pyrrole ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: 1-Benzyloctahydropyrrolo[3,4-b]pyrrole is used in the synthesis of intermediates as quinolone anti-bacterials.

Technology Process of 1-BENZYL-OCTAHYDRO-PYRROLO[3,4-B]PYRROLE

There total 3 articles about 1-BENZYL-OCTAHYDRO-PYRROLO[3,4-B]PYRROLE 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: 90.0%

ethyl 1-benzyl-octahydropyrrolo[2,3-c]pyrrole-5-carboxylate (132414-78-9,894853-99-7) → 1-benzyl-octahydropyrrolo[2,3-c]pyrrole (132414-50-7)

Guidance literature:

With hydrogenchloride; In water; for 24h; Reflux;

Reference yield:

ethyl N-(2,2-dimethoxyethyl)-N-(prop-2-en-1-yl)carbamate (128740-02-3) → 1-benzyl-octahydropyrrolo[2,3-c]pyrrole (132414-50-7)

Guidance literature:

Multi-step reaction with 3 steps

1: formic acid / 0.5 h / Reflux

2: toluene / 4 h / Reflux

3: hydrogenchloride / water / 24 h / Reflux

With hydrogenchloride; formic acid; In water; toluene;

Reference yield:

N-allyl-N-(2-oxoethyl)carbamic acid,ethyl ester (128740-03-4) → 1-benzyl-octahydropyrrolo[2,3-c]pyrrole (132414-50-7)

Guidance literature:

Multi-step reaction with 2 steps

1: toluene / 4 h / Reflux

2: hydrogenchloride / water / 24 h / Reflux

With hydrogenchloride; In water; toluene;

upstream raw materials:

ethyl 1-benzyl-octahydropyrrolo[2,3-c]pyrrole-5-carboxylate

ethyl N-(2,2-dimethoxyethyl)-N-(prop-2-en-1-yl)carbamate

N-allyl-N-(2-oxoethyl)carbamic acid,ethyl ester

Downstream raw materials:

7-(1-benzyl-hexahydro-pyrrolo[3,4-b]pyrrol-5-yl)-2-(4-bromo-phenyl)-oxazolo[5,4-d]pyrimidine

7-(1-benzyl-hexahydro-pyrrolo[3,4-b]pyrrol-5-yl)-2-(6-chloro-pyridin-3-yl)-oxazolo[5,4-d]pyrimidine

tert-butyl 1-benzyl-octahydropyrrolo[2,3-c]pyrrole-5-carboxylate

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