HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591966Generated: October 30, 2026
Triphenylphosphine → HCID 67138359, compound
https://huagongshe.com/reaction/1591966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Boc-4-aminobenzylalcohol | HCID 10242688 | — |
| Reactant | HCID 66751042 | HCID 66751042 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67138359 | HCID 67138359 | — |
Reaction Steps
The title B compound, 2-(2,4-dimethoxybenzyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (98 mg, 0.34 mmol) and (4-hydroxymethylphenyl)carbamic acid t-butyl ester (153 mg, 0.68 mmol) and triphenylphosphine (180 mg, 0.68 mmol) are dissolved in THF (10 mL) with stirring under argon atmosphere. The reaction is cooled in an ice/water bath and diethyl azodicarboxylate (0.107 mL, 0.68 mmol) dissolved in THF (0.107 mL) is added dropwise. After 16 h, the solvent is evaporated and the residue is taken up in a minimal amount of CH2Cl2 and chromatographed on silica gel with a gradient from 1 to 5% EtOAc in CH2Cl2 over 15 min to give {4-[5-(2,4-dimethoxybenzyl)-1,1,4-trioxo-1,2,5-thiadiazolidin-2-ylmethyl]-phenyl}-carbamic acid t-butyl ester as an oil: [M+NH4]+=509.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291635B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-302720bb3dc047c78112d4019be7f9d3 |
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| Source note | uspto-grants-2007_11 |
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