HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045101Generated: October 31, 2026
(4-Ethynylphenyl)methanol → HCID 178451390, compound
https://huagongshe.com/reaction/1045101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (4-Ethynylphenyl)methanol | HCID 11170993 | — |
| Reactant | Tert-butyl 2-(6-chloro-5-iodo-1H-benzo[d]imidazol-2-ylthio)acetate | HCID 58387110 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178451390 | HCID 178451390 | — |
Reaction Steps
A 2 mL Biotage™ microwave vial was charged with copper iodide (1.1 mg, 10 mol %), and Pd(PPh3)2Cl2 (2.1 mg, 5 mol %). A solution of (6-chloro-5-iodo-1H-benzoimidazol-2-ylsulfanyl)-acetic acid tert-butyl ester (Intermediate 4, 25.0 mg, 0.059 mmol) in DMF (0.5 mL) was added to the vial, followed by a solution of (4-ethynyl-phenyl)-methanol (15.0 mg, 0.118 mmol) in DMF (250 uL) and TEA (57 uL, 0.41 mmol). The resulting suspension was heated in a microwave synthesizer (Biotage Initiator™) at 120° C. for 5 min. The solvent was removed in vacuo to give dark brown oil which was used in the next step without further purification. LR-MS (API-ES): calculated for C22H21ClN2O3S 428.1, observed m/e 429.0 (M+H)+ (Rt 3.05 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563746B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-0cc11599284f48169d5bd6c5fbf8a528 |
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| Source note | uspto-grants-2013_10 |
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