HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678659Generated: November 2, 2026
Triphenylphosphine → HCID 67131198, compound
https://huagongshe.com/reaction/1678659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | Methyl 4-hydroxy-3,5-dimethylbenzoate | HCID 12389264 | — |
| Reactant | HCID 67131197 | HCID 67131197 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67131198 | HCID 67131198 | 27% |
Reaction Steps
To a solution of 2-[2-(4-chloro-phenyl)-2H-indazol-3-yl]-2-cyclohexyl-ethanol (20 mg, 56 umol) in THF (1 ml) was added 4-hydroxy-3,5-dimethyl-benzoic acid methyl ester (11 mg, 62 umol; CAS Reg. No. 34137-14-9) and tri-phenylphosphine (18 mg, 68 umol) at ambient temperature under an argon atmosphere. The mixture was cooled to 0° C., di-tert-butyl azodicarboxylate (16 mg, 68 umol) was added and the suspension was stirred for 14 h at ambient temperature. The solvent was removed under reduced pressure to give a solid which was purified by column chromatography (silica gel, iPrOAc/heptane) to obtain the title compound (8 mg, 15 umol; 27%) as colorless oil. MS: m/e=517.3 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008505B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-a54cd12794a440aaa6c31c1d9b2a1afd |
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| Source note | uspto-grants-2011_08 |
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