HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234875Generated: October 28, 2026
N-Hydroxyphthalimide → HCID 23353087, compound
https://huagongshe.com/reaction/234875
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 5-(4-Fluorophenyl)-4-pentyn-1-ol | HCID 18987996 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23353087 | HCID 23353087 | 82% |
Reaction Steps
33.4 g (0.205 mol) of N-hydroxyphthalimide and 53.8 g (0.205 mol) of triphenylphosphine were added to a solution of 33.1 g (0.186 mol) of 5-hydroxy-1-(4-fluorophenyl)-1-pentine in 430 ml of tetrahydrofuran. 35.7 g (0.205 mol) of diethyl azodicarboxylate were then added in the course of 2.5 hours with monitoring of the temperature (max. 40° C.). Stirring was carried out overnight at room temperature, the mixture was evaporated down under reduced pressure and the residue was taken up with 300 ml of dichloromethane. The solution was washed twice with sodium carbonate solution and once with saturated sodium chloride solution. After drying and evaporating down, the crude product was purified by chromategraphy over silica gel. The eluent used was initially dichloromethane/n-hexane and subsequently pure dichloromethane. Yield: 82%; mp.: 85°-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05597776 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-62a8d454f04d406ba642f72182331167 |
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| Source note | uspto-grants-1997_01 |
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