HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350854Generated: November 3, 2026
Ethyl bromoacetate → HCID 58640415, compound
https://huagongshe.com/reaction/1350854
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 23014065 | HCID 23014065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58640415 | HCID 58640415 | 67% |
Reaction Steps
To a stirred suspension of 60% sodium hydride (240 mg, 5.87 mmol) in anhydrous tetrahydrofuran (5 ml) was added a solution of crude 1,1-dimethylindan-5-ol (878 mg) in anhydrous tetrahydrofuran (10 ml) dropwise at 0° C. After 15 minutes at 0° C., to this was added ethyl bromoacetate (1.16 g, 6.94 mmol) via a syringe at 0° C. After 2 hours at ambient temperature, the mixtute was quenched with water (15 ml) and extracted with ethyl acetate. The combined solution was washed with brine, dried over sodium sulfate. After filtration to separate solvent and sodium sulfate, the solvent was removed under reduced pressure to give a residue, which was applied to a silica gel chromatography column and eluted with hexane/ethyl acetate=8/1–6/1 to furnish 890 mg (67% yield in 2 steps) of the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07214824B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-4b50cc47f1a843eba9b7498f9e7bdf90 |
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| Source note | uspto-grants-2007_05 |
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