HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367094Generated: October 31, 2026
Ethyl p-methylbenzenesulfonate → HCID 21345202, compound
https://huagongshe.com/reaction/367094
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl p-methylbenzenesulfonate | HCID 6638 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21345207 | HCID 21345207 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21345202 | HCID 21345202 | 98% |
Reaction Steps
A solution of 5-hydroxy-3-(1-Boc-2-(S)-azetidinylmethoxy)pyridine (500 mg, 1.78 mmol, from step 120f) in dimethylformamide (15 mL) was treated with ground KOH (170 mg, 1.7 mmol) and stirred for 30 minutes at room temperature. To this mixture was rapidly added ethyl p-toluenesulfonate (430 mg, 2.14 mmol), and the resultant was stirred at 80° C. overnight. The mixture was concentrated to remove the dimethylformamide, and the residue was diluted with water and extracted with EtOAc. The organic extracts were combined, dried (MgSO4), filtered and concentrated under vacuum to give 1.0 g of unpurified product. This material was purified by chromatography (silica gel: hexane/EtOAc, 1:1) to give 537 mg (98%) of the title compound. 1H NMR (CDCl3, 300 MHz) δ: 1.40 (s, 9H), 1.42 (t, J=6 Hz, 3H), 2.30 (m, 2H), 3.92 (t, J=9 Hz, 2H), 4.05 (q, J=6 Hz, 2H), 4.30 (m, 1H), 4.54 (m, 1H), 6.80 (m, 1H), 7.95 (m, 2H). MS (CI/NH3) m/e: 309 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133253 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-b4a9c91bb5254ecd9db147734cb8aa36 |
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| Source note | uspto-grants-2000_10 |
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