HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651537Generated: October 26, 2026
Triphenylphosphine → 2-Chlorobenzenesulfonic acid 3-[(3-cyanophenyl)methoxy]phenyl ester
https://huagongshe.com/reaction/651537
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 3-(Hydroxymethyl)benzonitrile | HCID 2734677 | — |
| Reactant | 2-Chlorobenzenesulfonic acid 3-hydroxyphenyl ester | HCID 54015281 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chlorobenzenesulfonic acid 3-[(3-cyanophenyl)methoxy]phenyl ester | HCID 53832837 | 93.8% |
Reaction Steps
Diethyl azodicarboxylate (174 mg, 1.0 mmol) was added to a solution of 2-chlorobenzenesulfonic acid 3-hydroxyphenyl ester (285 mg, 1.0 mmol), as prepared in the preceding step, 3-cyanobenzyl alcohol (133 mg, 1.0 mmol)(Yoon et al., J. Org. Chem. 38:2786-2792 (1973)), and triphenylphosphine (263 mg, 1.0 mmol) in tetrahydrofuran (10 mL) at 0° C. The mixture was stirred at 0° C. for 2 hours and at room temperature for 3 hours. The reaction mixture was quenched with water (30 mL) and extracted with ethyl acetate (3×30 mL). The organic phase was washed with saturated NaHCO3 (2×30 mL), brine (2×30 mL) and dried over Na2SO4. The solvent was removed in vacuo the residue was purified by flash column chromatography (2:1 ethyl acetate:hexane) to give the title compound as a pale yellow oil (375 mg, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06281206B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-a35914753ac746a2895154bb69708d29 |
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| Source note | uspto-grants-2001_08 |
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