HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579169Generated: October 30, 2026
1,2-Dibromo-1,1,2,2-tetrafluoroethane → HCID 66684882, compound
https://huagongshe.com/reaction/579169
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dibromo-1,1,2,2-tetrafluoroethane | HCID 31301 | — |
| Reactant | 5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid | HCID 58114072 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66684882 | HCID 66684882 | — |
Reaction Steps
To a of solution of 5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid (6.5 g, 31.3 mmol, 1.0 equiv) in THF (150 mL) at −78° C. was added n-BuLi (44.9 mL, 1.6 M in heptane, 71.9 mmol, 2.3 equiv) and the resulting solution was stirred at −78° C. for 1 hour. To the solution was then added 1,2-dibromo-1,1,2,2-tetrafluoro-ethane (16.2 g, 62.5 mmol, 2.0 equiv) and the solution was allowed to warm to room temperature over 2 hours. The reaction was quenched by addition of sat. aq. NH4Cl solution and the mixture was extracted with EtOAc. The organic layers were combined, washed with brine, dried over Na2SO4 and concentrated. The crude material was continued to the next step with no further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040690B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-1f9d8a1126914acc96736366e446cbe0 |
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| Source note | uspto-grants-2015_05 |
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