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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720117Generated: October 30, 2026

Ammonium Chloride → 3-Ethynylbenzenemethanol

https://huagongshe.com/reaction/720117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium FluorideHCID 522689—
Reactant3-(Trimethylsilyl)ethynylbenzaldehydeHCID 2771642—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-EthynylbenzenemethanolHCID 15468770—

Reaction Conditions

Temperature22 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132533B2
Source datasetuspto-grants-2006_11
ORD IDord-e870517df16449a9a7a25d74ab0bece6
Source noteuspto-grants-2006_11