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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63808Generated: October 29, 2026

Sodium ethoxide → 6,10,14-Trimethyl-pentadeca-5,9,13-trien-1-yne

https://huagongshe.com/reaction/63808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantTrimethyl-(6,10,14-trimethyl-pentadeca-5,9,13-trien-1-ynyl)-silaneHCID 73095183—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
Product6,10,14-Trimethyl-pentadeca-5,9,13-trien-1-yneHCID 7276580696%

Reaction Conditions

Temperature60 °C

Reaction Steps

A 3-N 250 mL flask was charged with trimethyl-(6,10,14-trimethyl-pentadeca-5,9,13-trien-1-ynyl)-silane (Ex-1B-7) (19.38 g, 64.1 mmol) and NaOEt (42 mL of a 21% w/w solution, 112 mmol). The reaction mixture was stirred at 60° C. for 4 h. After cooling to RT, the reaction mixture was diluted with MTBE (100 mL) and water (100 mL) and then filtered to remove solid present at the phase interface. The aqueous layer was extracted with MTBE (3×100 mL). The combined MTBE layers were washed with brine (100 mL), dried over MgSO4, filtered, and concentrated by rotary evaporation to yield 12.43 g of 6,10,14-trimethyl-pentadeca-5,9,13-trien-1-yne (Ex-1B-8) as a dark orange oil (96%). 1H NMR (400 MHz, CDCl3) δ (ppm): 5.23-5.17 (m, 1H), 5.17-5.07 (m, 2H), 2.29-1.95 (m, 13H), 1.70 (s, 3H), 1.65 (s, 3H), 1.62 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447006B2
Source datasetuspto-grants-2016_09
ORD IDord-5d73db12900d4e17adc23f9f8043f057
Source noteuspto-grants-2016_09