HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192740Generated: November 1, 2026
3-Hydroxybenzyl alcohol → 3-(2-Propyn-1-yloxy)benzenemethanol
https://huagongshe.com/reaction/1192740
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Hydroxybenzyl alcohol | HCID 102 | — |
| Reactant | 3-Chloro-1-propyne | HCID 12221 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-Propyn-1-yloxy)benzenemethanol | HCID 10797067 | 60% |
Reaction Steps
A 20.0 L flange flask was charged with 3-hydroxybenzyl alcohol (97%, ex. Aldrich, 903 g, 7.28 mol, 1 eq.) in methanol (MeOH)(9.1 L, dried over 3 A molecular sieves) to give a clear solution, into which sodium methoxide (25% in methanol, ex. Aldrich, 1.746 L, 7.63 mol, 1.05 eq.) was slowly added with vigorous stirring. After stirring for 10 min. the propargyl chloride (70 wt % in toluene, ex. Aldrich, 542.6 g, 805 ml, 7.29 mol, 1 eq) was added slowly with vigorous stirring over a period of 30 minutes. The reaction mixture was heated under reflux for 40 h (isomantle set to 76° C. with an internal temp. of 64° C.). TLC-examination (10% MeOH in DCM) showed that the reaction was not complete. The reaction was nevertheless worked-up at this stage. The MeOH was removed by rotary evaporation, and the residue dissolved in DCM (10.2 L) to give a clear solution, which was washed with water (5.82 L×3), and dried over sodium sulfate. The solvent was removed in vacuo, to give the title compound (706 g, 60%) as an orange gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680265B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-ee0590c068744ee8af4566d81bfc9896 |
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| Source note | uspto-grants-2014_03 |
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