Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,3-DithianeHCID 10451—
Reactant5-Bromo-1-indanoneHCID 520695—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5-bromo-1-(1,3-dithian-2-yl)-2,3-dihydro-1H-inden-1-olHCID 57419484100%

Reaction Conditions

Temperature-15 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139536B2
Source datasetuspto-grants-2015_09
ORD IDord-4da8b961396b41438095f60fc36f0b12
Source noteuspto-grants-2015_09