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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064147Generated: October 30, 2026

Ammonium Chloride → 3-Ethynylbenzenemethanol

https://huagongshe.com/reaction/1064147

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 numberUS06967198B2
Source datasetuspto-grants-2005_11
ORD IDord-bab7b1d427fd4f5a9c0e587b366cdf1a
Source noteuspto-grants-2005_11