HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299196Generated: October 30, 2026
Ethyl bromoacetate → Ethyl (+/-) 3-(3-methoxyphenyl)indeneacetate
https://huagongshe.com/reaction/2299196
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 3-(3-Methoxyphenyl)indene | HCID 15621211 | — |
| Reactant | HCID 178418261 | HCID 178418261 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (+/-) 3-(3-methoxyphenyl)indeneacetate | HCID 18340686 | 19.8% |
Reaction Steps
To a cold solution of 3-(3-methoxyphenyl)indene (4 g, 18 mmol), prepared by the method of J. Med. Chem. 1981, 24, 998, in THF (15 mL) at 0° C. was added dropwise a solution of LiN(TMS)2 (20 mL, 1M in THF) over 5 min. The resulting solution was added dropwise to a solution of ethyl bromoacetate (3.34 g, 20 mmol) in THF (15 mL) at −78° C. over 30 min. After 2.5 h, the mixture was quenched with saturated ammonium chloride solution and the layers were separated. The organic layer was dried over MgSO4 and concentrated to give the crude product which was purified by column chromatography (SiO2/2-4% EtOAc/hexane) to give title compound (1.1 g): 1H NMR (400 MHz, CDCl3) δ1.30 (t, 3H), 2.50 (m, 1H), 2.85 (m, 1H), 3.85 (s, 3H), 4.0 (m, 1H), 4.20 (q, 2H), 6.6 (s, 1H), 6.9 (m, 1), 7.2 (s, 1H), 7.35 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495560B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-0e0cb656a40f44b0b3218516c3088ed3 |
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| Source note | uspto-grants-2002_12 |
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