HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096828Generated: October 26, 2026
p-Toluenesulfonic acid → 2-(Thiazol-2-yloxy)ethanol
https://huagongshe.com/reaction/1096828
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-[2-(Tert-butyldimethylsilanyloxy)ethoxy]thiazole | HCID 66784256 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Thiazol-2-yloxy)ethanol | HCID 45121950 | 65% |
Reaction Steps
para-Toluenesulfonic acid (11.2 g, 58.0 mmol) was added to a sol. of 2-[2-(tert-butyldimethylsilanyloxy)ethoxy]thiazole (15.0 g, 58.0 mmol) in MeOH (300 mL) at 0° C. The mixture was stirred for 2 h at 0° C. Aq. sat. NaHCO3 was added until a pH of 6-7 was reached. The solvents were partially removed under reduced pressure, and the residue was diluted with EtOAc. The mixture was washed with aq. sat. NaHCO3 (1×), and the aq. phase was extracted back with EtOAc (1×). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the crude by FC (EtOAc/heptane 1:1) yielded the title compound (5.43 g, 65%). LC-MS: tR=0.48 min, ES+: 146.09.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138340B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-9f15072f02ab48f599a29b040cd8b7e1 |
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| Source note | uspto-grants-2012_03 |
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