HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716319Generated: October 29, 2026
1,4-Dibromobutane → N-(4-Bromo-butyl)-2-(4-fluoro-phenylsulfanyl)-N-trityloxy-acetamide
https://huagongshe.com/reaction/1716319
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-(4-Fluoro-phenylsulfanyl)-N-trityloxy-acetamide | HCID 86619939 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(4-Bromo-butyl)-2-(4-fluoro-phenylsulfanyl)-N-trityloxy-acetamide | HCID 86619940 | — |
Reaction Steps
To a solution of 2-(4-fluoro-phenylsulfanyl)-N-trityloxy-acetamide (132.1 mg, 0.228 mmol) from step C and Cs2CO3 (125.6 mg, 0.385 mmol) in anhydrous DMF (3 mL) was added 1,4-dibromo-butane (0.2 ml, 364.8 mg) in one portion and the resulting solution was warmed to 60° C. After TLC indicated the completion of the reaction (<30 min), the reaction mixture was diluted with EtOAc and washed sequentially with water and saturated NaCl solution. The organic phase was then dried over anhydrous Na2SO4 and concentrated under reduced pressure to give a crude material, which was then used in next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803793B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-6d4ecc6ee2ce4d8ba6bbc64b3c4449ab |
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| Source note | uspto-grants-2010_09 |
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