HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269452Generated: October 27, 2026
Sodium borohydride → 7-Bromo-2-isopropyl-1H-indene
https://huagongshe.com/reaction/269452
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Reactant | 2-Isopropyl-4-bromo-1-indanone | HCID 22173019 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Bromo-2-isopropyl-1H-indene | HCID 59832518 | — |
Reaction Steps
To a solution of 73.4 g (0.29 mol) of 4-bromo-2-isopropylindan-1-one in 530 ml of a mixture of THF-methanol (2:1, vol.), 22.0 g (0.58 mol) 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 600 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 1500 ml of toluene, and 2.0 g of p-TosOH was added. The resulting solution was refluxed for 2 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 vacuum distillation (bp 128-132° C./4 mm Hg). Yield 57.8 g (84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446216B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-89c545b53027434b91dbc8ec21561750 |
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| Source note | uspto-grants-2008_11 |
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