HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956173Generated: November 1, 2026
3-Fluorobenzyl bromide → HCID 23226992, compound
https://huagongshe.com/reaction/1956173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluorobenzyl bromide | HCID 68007 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Reactant | HCID 178422611 | HCID 178422611 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 23226992 | HCID 23226992 | — |
Reaction Steps
A mixture of 0.57 g (0.002 mol) of 4-mercapto-5-(2,2-dimethylindan-1-yl)pyrimidine, 0.57 g (0.003 mol) of 3-fluorobenzyl bromide, and 0.41 g (0.003 mol) in 10 mL of acetonitrile was stirred at ambient temperature for 2 hr. Saturated aqueous ammonium carbonate (5 mL) was added and the mixture obtained was extracted with ethyl acetate. The extract solution was washed with water and with concentrated aqueous sodium chloride and then was dried over sodium sulfate and concentrated by evaporation under reduced pressure. The resulting oil was low pressure liquid chromatographed on silica gel eluting first with hexane and then with a 20:80 by volume mixture of ethyl acetate and hexane. The eluent fractions containing the major component were concentrated by evaporation under reduced pressure to obtain the title compound as a white solid melting at 60°-62° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05780465 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-9e74268ea6294dd695862118decfbd08 |
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| Source note | uspto-grants-1998_07 |
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