HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224922Generated: October 30, 2026
Methyl phenylacetate → HCID 68870927, compound
https://huagongshe.com/reaction/2224922
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl phenylacetate | HCID 7559 | — |
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | (Bromomethyl)cyclobutane | HCID 2734658 | — |
| Reactant | Lithium diisopropylamine | HCID 45051747 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | HCID 68870927 | HCID 68870927 | — |
Reaction Steps
To a stirring solution of freshly prepared lithium diisopropylamine (76.5 mmol) in 500 mL of tetrahydrofuran at 0° C. was added methyl phenylacetate (10.44 g, 69.50 mmol) in 125 mL tetrahydrofuran dropwise over 30 minutes. After stirring at 0° C. for 1 hour the reaction mixture was cooled to −78° C. and treated with 50 mL of hexamethylphosphoric triamide followed by the dropwise addition of bromomethyl cyclobutane (9.37 mL, 83.4 mmol) and LiI (200 mg). The reaction mixture was stirred for 18 hours warming to 25° C. The reaction was quenched over 1 L of water containing 250 mL of sat. NH4Cl and extracted 3× with ethyl acetate. The combined organic layers were washed sequentially with saturated sodium bicarbonate, brine, and dried over MgSO4 yielding the crude product as an oil that was used without further purification. 1H NMR (300 MHz, CDCl3): δ ppm 1.59 m, 2 H) 1.89 m, 5 H) 2.17 m, 2 H) 3.47 (t, J=7.54 Hz, 1 H) 3.64 (s, 3 H) 7.31 (m, 5 H). MS (ESI+) m/z=236 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07378414B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-ea5c2f19af4c46b184c6068821e1c4c2 |
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| Source note | uspto-grants-2008_05 |
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