HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176163Generated: November 1, 2026
Triphenylphosphine → HCID 68408307, compound
https://huagongshe.com/reaction/1176163
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Benzene, 1-(dodecyloxy)-4-iodo- | HCID 10883601 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Piperidine | HCID 8082 | — |
| Product | HCID 68408307 | HCID 68408307 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07842758B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-06155a86bd304016abeaf05e10819f05 |
|---|
| Source note | uspto-grants-2010_11 |
|---|