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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461012Generated: November 2, 2026

Propargyl alcohol → HCID 18176104, compound

https://huagongshe.com/reaction/1461012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantSodium hydrideHCID 24758—
Reactant10-Bromodecanoic AcidHCID 142712—
ProductHCID 18176104HCID 1817610414%

Reaction Conditions

Temperature25 °C

Reaction Steps

Sodium hydride (420 mg, 8.75 mmol) was added to propargyl alcohol (68 mL, 1.17 mol) at 4° C. and stirred for 30 minutes at 25° C. 10-Bromodecanoic acid (2g, 7.96 mmol) was added to this mixture and the reaction was stirred at 98° C. for 48 hrs. The reaction mixture was extracted with water and ethyl acetate at pH 1. After drying the organic phase over sodium sulfate, the solvent was removed at reduced pressure. Product was purified over silica gel chromatography in 7-10% ethyl acetate/hexane/0.3% formic acid and then over a second silica gel column in 1-2.5% ethyl acetate/benzene/0.3% formic acid to yield 10-(2-propynoxy)decanoic acid (245 mg, 14%). mp <30° C.; 1H NMR (300 MHz, CDC13) δ 1.25-1.42 (br, 10H, methylene envelope), 1.54-1.70 (bm, 4H, OCH2CH2, CH2CH2COOH), 2.35 (t, 2H, J=7.4, CH2COOH), 2.43 (t, 1H, J=2.3, HC=C), 3.52 (t, 2H, J=6.8, OCH2), 4.14 (d, 2H, J=2.5, C=CCH2O), 10.42 (br, 1H, COOH); 13C NMR (75.4 MHz, CDC13) δ 24.68, 26.06, 29.04, 29.17, 29.35*, 29.46, 34.09, 57.95, 70.22, 74.09, 79.90, 180.02; m/z 227 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05073571
Source datasetuspto-grants-1991_12
ORD IDord-4ab701fd254242508c70b073a1c80178
Source noteuspto-grants-1991_12