HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720117Generated: October 30, 2026
Ammonium Chloride → 3-Ethynylbenzenemethanol
https://huagongshe.com/reaction/720117
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 3-(Trimethylsilyl)ethynylbenzaldehyde | HCID 2771642 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Ethynylbenzenemethanol | HCID 15468770 | — |
Reaction Steps
To 3-trimethylsilanylethynyl-benzaldehyde 73(a1) from step 1a in methanol (540 mL, 0.3 M) was added KF (18.8 g, 324 mmol), and the resulting mixture stirred at 22° C. for 6 hours. After cooling to 0° C., NaBH4 (6.13 g, 162 mmol) was carefully added over 0.5 hours. Aqueous saturated NH4Cl was carefully added and the volatiles were removed in vacuo. Ethyl acetate (200 mL) was added, and the organic phase was washed with water and a saturated aqueous NaCl solution, dried over MgSO4 and filtered. The volatiles were removed in vacuo to afford crude (3-ethynyl-phenyl)-methanol 73(a2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132533B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-e870517df16449a9a7a25d74ab0bece6 |
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| Source note | uspto-grants-2006_11 |
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