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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176163Generated: November 1, 2026

Triphenylphosphine → HCID 68408307, compound

https://huagongshe.com/reaction/1176163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantBenzene, 1-(dodecyloxy)-4-iodo-HCID 10883601—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventPiperidineHCID 8082—
ProductHCID 68408307HCID 68408307—

Reaction Conditions

Temperature50 °C

Reaction Steps

4-(Dodecyloxy)iodobenzene (4.04 g, 1.04×10−2 mol), triphenylphosphine (0.165 g, 6.29×10−4 mol), CuI (0.108 g, 5.67×10−4 mol) and Pd(PPh3)2Cl2 (0.153 g, 2.18×10−4 mol) were dissolved in 40 ml of dry piperidine under N2. (Trimethylsilyl)acetylene (3.00 ml, 2.12×10−2 mol) was added and the mixture was stirred at 50° C. for 6 h under N2. After cooling, the reaction mixture was poured into aq. NH4Cl and extracted with CH2Cl2 (three times). The combined organic layers were washed with aq. NH4Cl, water, and dried over Na2SO4. The crude product was chromatographed on silica gel with 4:1 hexane:CH2Cl2 as the eluent. Yield=3.633 g (97% based on 4.04 g of 4-(dodecyloxy)iodobenzene). 1H NMR (250 MHz, CDCl3): δ 7.39 (d, 2H, J=8.9 Hz, Ph), 6.80 (d, 2H, J=9.0 Hz, Ph), 3.94 (t, 2H, J=6.6 Hz, —OCH2—), 1.77 (quint, 2H, J=6.6 Hz, —OCH2CH2—), 1.17-1.50 (m, 18H, —CH2—), 0.88 (t, 3H, J=6.6 Hz, —CH3), 0.24 (s, 9H, Si—CH3). CI MS m/z: 358.268 (M+) (calcd 358.269).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842758B2
Source datasetuspto-grants-2010_11
ORD IDord-06155a86bd304016abeaf05e10819f05
Source noteuspto-grants-2010_11