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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269448Generated: October 29, 2026

Sodium borohydride → HCID 58975411, compound

https://huagongshe.com/reaction/269448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMeOH tetrahydrofuranHCID 21899815—
ReactantHCID 59832534HCID 59832534—
SolventWaterHCID 962—
ProductHCID 58975411HCID 58975411—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 32.5 g (136 mmol) of 4-bromo-2,6-dimethylindan-1-one in 370 ml of a mixture of THF-methanol (2:1, vol.), 11.8 g (312 mmol) of NaBH4 was added in small portions while vigorously stirring for 2 h at 0° C. This mixture was stirred for 12 h at room temperature and then added to 1000 ml of cold water. The organic layer was separated, the aqueous layer was extracted with 3×300 ml of methyl-tert-butyl ether. The combined organic fractions were dried over K2CO3 and then evaporated to dryness. The residue was dissolved in 700 ml of toluene, and 2.0 g of p-TosOH was added. The resulting solution was refluxed for 1 h using a Dean-Stark trap to remove the water formed, and then it was passed through a short Silica Gel 60 column (40-63 um, d 100 mm, l 80 mm, eluent: hexanes). This column was additionally washed with 250 ml of toluene. The combined organic fractions were evaporated to dryness. The product was isolated by flash chromatography on Silica Gel 60 (40-63 um, d 60 mm, l 150 mm, eluent: hexanes). Yield 24.6 g (81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446216B2
Source datasetuspto-grants-2008_11
ORD IDord-ececa324a3ee427bb69abf74f7a94487
Source noteuspto-grants-2008_11