HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531894Generated: October 25, 2026
Sodium hydride → 9-(Benzenesulfonyl)-1-bromocarbazole
https://huagongshe.com/reaction/531894
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Iodobenzene-1-sulfonyl chloride | HCID 627400 | — |
| Reactant | 1-Bromo-9H-carbazole | HCID 11230335 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 9-(Benzenesulfonyl)-1-bromocarbazole | HCID 67405182 | — |
Reaction Steps
19.6 g (80 mmol) of 1-bromocarbazole are initially introduced in 1000 ml of THF, and 8.9 g (223.3 mmol) of NaH (60% in oil) are added at 0° C. 24 g (80 mmol) of 2-iodobenzenesulfonyl chloride are subsequently added to the mixture, which is then stirred at 40° C. for 12 h. The organic phase is dried over MgSO4, and the solvent is removed in vacuo. The residue is recrystallised from acetone and finally sublimed in a high vacuum. Yield: 29 g (574 mmol), 72% of theory, purity according to HPLC 99.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09356243B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-87e5b73f9cee4b63a3a7b17838d7769f |
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| Source note | uspto-grants-2016_05 |
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