HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323302Generated: October 26, 2026
Tetrahydrofuran → HCID 18464502, compound
https://huagongshe.com/reaction/323302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Benzenepropanenitrile | HCID 12581 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | tert-Butyl(2-iodoethoxy)dimethylsilane | HCID 11129873 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 18464502 | HCID 18464502 | — |
Reaction Steps
Combine 3-phenylpropionitrile (2.0 g, 15.25 mmol) and tetrahydrofuran (15 mL). Cool to −78° C. using a dry-ice/acetone bath. Add a solution of lithium bis(trimethylsilyl)amide (16.0 mL, 1 M in THF, 16.0 mmol). After 1 hour, add 2-(t-butyldimethylsilyloxy)ethyl iodide (4.58 g, 16.0 mmol). After the addition of 2-(t-butyldimethylsilyloxy)ethyl iodide is complete, warm slowly to ambient temperature over about 7 hours. Add water and extract twice with ethyl acetate. Dry the combined organic layers over Na2SO4, filter, and concentrate in vacuo to obtain a residue. Chromatograph the residue on silica gel eluting with 5% ethyl acetate/hexane to give the title compound: Rf=0.50 (silica gel, 10% ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06211199B1 |
|---|
| Source dataset | uspto-grants-2001_04 |
|---|
| ORD ID | ord-c984d5919abb4204beeca79607e9afa6 |
|---|
| Source note | uspto-grants-2001_04 |
|---|