Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786522Generated: October 29, 2026

Hydrochloric Acid → HCID 69036788, compound

https://huagongshe.com/reaction/1786522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant6-Bromospiro[2H-1-benzopyran-2,1′-cyclopentan]-4(3H)-oneHCID 59167871—
SolventMethanolHCID 887—
ProductHCID 69036788HCID 69036788—

Reaction Steps

Sodium borohydride (4.65 g, 0.123 mol) was added to a stirred suspension of 6-bromo-3,4-dihydro-spiro[2H-1-benzopyran-2,1′-cyclopentan]-4-one (31.83 g, 0.1137 mol) in methanol (650 mL) at 0° C. and the mixture was maintained at this temperature for a further 30 minutes. After stirring for an additional 30 minutes at room temperature, concentrated hydrochloric acid was added until acid and the solvent was evaporated under reduced pressure. Water was added to the residue and the product was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and evaporated under reduced pressure. The crude product was recrystallized from diethylether/petroleum ether 40-60° C. (⅓). The resulting precipitate was collected by filtration, washed with petroleum ether and dried (71%). mp: 123-123.5° C., IR (KBr): 3271 (O—H), 2963, 2873 (C—H aliphatic) cm−1, Anal. (C13H15O2Br) C, H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507761B2
Source datasetuspto-grants-2009_03
ORD IDord-f0f4ba2f76c247f393accfad4465076f
Source noteuspto-grants-2009_03