HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004180Generated: October 31, 2026
Triphenylphosphine → HCID 23434069, compound
https://huagongshe.com/reaction/1004180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | tert-Butyl (((1,1-dimethylethoxy)carbonyl)oxy)carbamate | HCID 2728863 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | HCID 23434113 | HCID 23434113 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23434069 | HCID 23434069 | 35.6% |
Reaction Steps
To a stirred solution of 3-hydroxymethyl-2,5-di(4-pyridyl)-4-methylthiophene (0.282 g), triphenylphosphine(0.446 g), and N,O-di-(tert-butoxycarbonyl)hydroxylamine (0.224 g), in THF (20 mL) was added diethylazodicarboxylate (0.296 g) under nitrogen. After stirring for 23 hours, the reaction mixture was poured into water (50 mL) and the whole was extracted with CH2Cl2 (100 mL). The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-CH2Cl2 -MeOH (1:1:0.04). The resulting product was purified by column chromatography on silica(NH-silica gel, FUJI SILISIA CHEMICAL LTD. DM203 5)(ethyl acetate-CH2Cl2 --MeOH=1:1:0.04) to give the subtitle compound (0.17 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06048880 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-c88815f3437048b3866b77d0f3a83321 |
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| Source note | uspto-grants-2000_04 |
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