• Product NameN-(Hydroxymethyl)phthalimide
  • CasNo. 118-29-6
  • MFC9H7NO3
  • MW177.159
  • Purity
  • Appearancewhite crystalline powder
  • Packing
  • Contact usInquiry

Product Details

CasNo: 118-29-6

MF: C9H7NO3

Appearance: white crystalline powder

Chinese Factory Supply Best Quality 118-29-6 with Cheap Price

  • Molecular Formula:C9H7NO3
  • Molecular Weight:177.159
  • Appearance/Colour:white crystalline powder 
  • Vapor Pressure:5.96E-05mmHg at 25°C 
  • Melting Point:147-149 °C 
  • Refractive Index:1.644 
  • Boiling Point:332 °C at 760 mmHg 
  • PKA:13.17±0.10(Predicted) 
  • Flash Point:154.6 °C 
  • PSA:57.61000 
  • Density:1.462 g/cm3 
  • LogP:0.17030 

N-(Hydroxymethyl)phthalimide(Cas 118-29-6) Usage

Definition

ChEBI: A primary alcohol comprising phthalimide carrying an N-hydroxymethyl substituent.

Preparation

To a flask equipped with a mechanical stirrer and condenser is added 511 gm (3.47 moles) of phthalimide, 260 ml of 40% formalin (3.47 moles), and 1750 ml of water. The mixture is refluxed for about 5-10 min or until a clear solution results (if any insoluble material remains, it is first filtered). Then the mixture is cooled for several hours. The resulting product is filtered with suction, washed with cold water, and air-dried to afford 594 gm (96%), m.p. 137-141°C. NOTE: The product should not be oven-dried since it decomposes with the loss of formaldehyde. Recrystallization of the product from ethanol affords 94% recovery of the original material with the same melting point range.

Synthesis Reference(s)

Journal of the American Chemical Society, 77, p. 1913, 1955 DOI: 10.1021/ja01612a068

InChI:InChI=1/C9H7NO3/c11-5-10-8(12)6-3-1-2-4-7(6)9(10)13/h1-4,11H,5H2

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Synthetic method N - hydroxymethyl phthalimide

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118-29-6 Process route

2-(iodomethyl)isoindoline-1,3-dione
203255-55-4

2-(iodomethyl)isoindoline-1,3-dione

N-methylphthalimide
550-44-7

N-methylphthalimide

2-(hydroxymethyl)-1H-isoindole-1,3(2H)-dione
118-29-6

2-(hydroxymethyl)-1H-isoindole-1,3(2H)-dione

1,3,4,5-tetrahydro-2,4-benzoxazepine-1,5-dione
1380112-97-9

1,3,4,5-tetrahydro-2,4-benzoxazepine-1,5-dione

Conditions
Conditions Yield
With diethylzinc; In hexane; dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
39%
14%
22%
2-(2-Hydroperoxy-2-methoxy-ethyl)-isoindole-1,3-dione
124536-28-3

2-(2-Hydroperoxy-2-methoxy-ethyl)-isoindole-1,3-dione

N-methylphthalimide
550-44-7

N-methylphthalimide

2-(hydroxymethyl)-1H-isoindole-1,3(2H)-dione
118-29-6

2-(hydroxymethyl)-1H-isoindole-1,3(2H)-dione

N-phthaloylglycine methyl ester
23244-58-8

N-phthaloylglycine methyl ester

Conditions
Conditions Yield
In dimethyl sulfoxide; Irradiation;
35%
40%
15%

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