1H-Isoindole-1,3(2H)-dione, 2-butoxy-

Base Information

• Chemical Name: 1H-Isoindole-1,3(2H)-dione, 2-butoxy-
• CAS No.: 51951-28-1
• Molecular Formula: C12H13NO3
• Molecular Weight: 219.24
• DSSTox Substance ID: DTXSID10484271
• Nikkaji Number: J1.805.230J
• Wikidata: Q82322512
• Mol file: 51951-28-1.mol

Synonyms:2-butoxy-1H-isoindole-1,3(2H)-dione;1H-Isoindole-1,3(2H)-dione, 2-butoxy-;N-Butoxyphthalimide;51951-28-1;2-butoxy-isoindole-1,3-dione;SCHEMBL14560518;DTXSID10484271;JCEKIQIXCILAPX-UHFFFAOYSA-N;AKOS003631127

Chemical Property of 1H-Isoindole-1,3(2H)-dione, 2-butoxy-

Chemical Property:

• PSA: 46.61000
• LogP: 1.95220
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 219.08954328
• Heavy Atom Count: 16
• Complexity: 266

Purity/Quality:

2-BUTOXY-1H-ISOINDOLE-1,3(2H)-DIONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCON1C(=O)C2=CC=CC=C2C1=O

Technology Process of 1H-Isoindole-1,3(2H)-dione, 2-butoxy-

There total 7 articles about 1H-Isoindole-1,3(2H)-dione, 2-butoxy- 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: 98.0%

N-hydroxyphthalimide (524-38-9) + butan-1-ol (71-36-3) → 2-butoxyisoindoline-1,3-dione (51951-28-1)

Guidance literature:

With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; for 16h; Ambient temperature;

DOI:10.1021/jm9607921

Reference yield: 95.0%

N-hydroxyphthalimide (524-38-9) + 1-iodo-butane (542-69-8) → 2-butoxyisoindoline-1,3-dione (51951-28-1)

Guidance literature:

With 1,8-diazabicyclo[5.4.0]undec-7-ene; In N,N-dimethyl-formamide; at 60 ℃; for 2h; Inert atmosphere;

Reference yield: 90.0%

1-bromo-butane (109-65-9) + N-hydroxyphthalimide (524-38-9) → 2-butoxyisoindoline-1,3-dione (51951-28-1)

Guidance literature:

With potassium carbonate; In dimethyl sulfoxide; at 20 - 55 ℃; for 3h;

upstream raw materials:

1-bromo-butane

N-hydroxyphthalimide

butan-1-ol

n-Butyl chloride

Downstream raw materials:

2,3-dihydrophthalazine-1,4-dione

O-n-butylhydroxylamine

butoxyamine hydrochloride

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