HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269425Generated: October 26, 2026
Pyridine 4-methylbenzene-1-sulfonate → 7-Phenylhept-6-yn-1-ol
https://huagongshe.com/reaction/269425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine 4-methylbenzene-1-sulfonate | HCID 161440 | — |
| Reactant | 2-(7-phenylhept-6-ynyloxy)tetrahydro-2H-pyrane | HCID 58924678 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-Phenylhept-6-yn-1-ol | HCID 58924679 | 97% |
Reaction Steps
Pyridine toluene-4-sulphonate (0.75 g, 3 mmol) was added to a magnetically stirred solution of 2-(7-phenylhept-6-ynyloxy)-tetrahydro-2H-pyrane (7) (13.62 g, 50 mmol) in dry methanol (300 mL). The reaction mixture was stirred at 55° C. and monitored by TLC. When all the base material had been converted, methanol was distilled out on a rotary evaporator and water (200 mL) was added to the residue. The aqueous phase was extracted with petroleum ether (boiling point 40-60° C.)/Et2O 1:1 (5×50 mL). The combined organic phases were washed with water (2×20 mL) and dried (MgSO4). Distillation on a rotary evaporator yielded 9.1 g (97%) of a yellow viscous oil. TLC and NMR indicated a pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446226B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-2facfffb0e2d44a9892ae3ed367c9f35 |
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| Source note | uspto-grants-2008_11 |
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