HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280614Generated: October 26, 2026
Hydrochloric Acid → 5-bromo-1-(1,3-dithian-2-yl)-2,3-dihydro-1H-inden-1-ol
https://huagongshe.com/reaction/2280614
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,3-Dithiane | HCID 10451 | — |
| Reactant | 5-Bromo-1-indanone | HCID 520695 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-bromo-1-(1,3-dithian-2-yl)-2,3-dihydro-1H-inden-1-ol | HCID 57419484 | 100% |
Reaction Steps
A solution of 1,3-dithiane (11.96 g, 99 mmol) in anhydrous tetrahydrofuran (100 mL) at −30° C. was treated dropwise over 10 min with n-butyllithium (2.5M in hexanes, 38.4 mL, 96 mmol) followed by stirring at −15° C. for 2 h. The solution was then treated with a solution of 5-bromo-2,3-dihydro-1H-inden-1-one (15 g, 71.1 mmol) in anhydrous tetrahydrofuran (250 mL) over 1 h, maintaining the temperature between −9° C. and 2° C. The mixture was then allowed to set in the refrigerator at 2-8° C. for 18 h. The solution was concentrated in vacuo to afford a maroon oil, which was treated with 1 N hydrochloric acid solution and extracted with ether. The ether layer was extracted with saturated sodium chloride solution, dried (Na2SO4) and concentrated in vacuo to afford an amber oil (23.55 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139536B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-4da8b961396b41438095f60fc36f0b12 |
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| Source note | uspto-grants-2015_09 |
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