HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539270Generated: October 30, 2026
Bis(2-bromoethyl) ether → 6-Bromo-2',3',5',6'-tetrahydrospiro[indene-2,4'-pyran]-1(3H)-one
https://huagongshe.com/reaction/539270
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(2-bromoethyl) ether | HCID 21521 | — |
| Reactant | 1-Indanone, 6-bromo- | HCID 139778 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Product | 6-Bromo-2',3',5',6'-tetrahydrospiro[indene-2,4'-pyran]-1(3H)-one | HCID 58198105 | 24.2% |
Reaction Steps
A solution of potassium tert-butoxide (3.94 g, 35.1 mmol) in t-BuOH (35 mL) was added dropwise over 15 min to a solution of 6-bromo-1-indanone (3.53 g, 16.73 mmol) in 2-methyl-tetrahydrofuran (350 mL) at r.t. under a nitrogen atmosphere. After 15 min bis(2-bromoethyl)ether (2.102 mL, 16.73 mmol) was added and the resulting mixture was stirred at r.t. for 5 h. Potassium tert-butoxide (0.938 g, 8.36 mmol) was added and the mixture was stirred at r.t. overnight. The mixture was quenched with saturated aq. NH4Cl (150 mL) and the organic layer was separated. The aqueous layer was extracted with EtOAc (3×50 mL) and Et2O (50 mL). The combined organics were washed with brine (100 mL), dried over MgSO4, filtered and concentrated. The resulting residue was taken up in DCM, concentrated onto silica gel and purified on a silica gel column eluted with 0-40% EtOAc in heptane to give 1.14 g (24% yield) of the title compound; MS (ES+) m/z 281 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865911B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c381d1a8670e494d8c036da79b987bd7 |
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| Source note | uspto-grants-2014_10 |
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