HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960138Generated: October 31, 2026
Triphenyl phosphite → HCID 67448110, compound
https://huagongshe.com/reaction/1960138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenyl phosphite | HCID 7540 | — |
| Reactant | (3-Bromophenyl)acetic acid | HCID 74653 | — |
| Reactant | 1,1'-Biphenyl-4-yl-boronic acid | HCID 151253 | — |
| Reactant | 4-Chloro-5-iodobenzene-1,2-diamine | HCID 57481467 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 67448110 | HCID 67448110 | — |
Reaction Steps
To a microwave vial containing a solution of Intermediate 11-1 (which was prepared from 5-chloro-4-iodo-1,2-phenylenediamine (Intermediate 1-6 of Example 1) and 4-biphenylboronic acid following the procedures of Step 9 in Example 1) (500 mg, 1.7 mmol) in pyridine 8 mL was added 3-bromo-phenyl acetic acid (365 mg, 1.7 mmol), followed by triphenyl phosphite (0.58 mL, 2.2 mmol). The reaction was run in a microwave reactor at 220° C. for 10 min. The solvent was partially removed in vacuo, then diluted with EtOAc (75 mL) and washed three times with 50 mL portions of saturated aqueous ammonium chloride. The combined organic layers were dried (MgSO4), filtered, concentrated in vacuo, and then purified by chromatography over silica (eluting with EtOAc/Hexanes=1/1) to give the title compound 14-1 as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410284B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-839953d6c0214a98ae0d30b7060073c7 |
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| Source note | uspto-grants-2013_04 |
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