HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234666Generated: October 26, 2026
5H-Dibenzo[a,d]cyclohepten-5-one → 5-cyclopropyl-5H-dibenzo[a,d]cyclohepten-5-ol
https://huagongshe.com/reaction/234666
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5H-Dibenzo[a,d]cyclohepten-5-one | HCID 16679 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-cyclopropyl-5H-dibenzo[a,d]cyclohepten-5-ol | HCID 18799338 | — |
Reaction Steps
A solution of cyclopropylmagnesium bromide in dry THF (prepared from cyclopropylbromide (8.0 g, 0.067 mol), magnesium turnings (1.3 g, 0.053 mol) and dry THF (35 ml)) was placed under an atmosphere of nitrogen. A solution of 5H-dibenzo[a,d]cyclohepten-5-one (6.0 g, 0.028 mol) in dry THF (15 ml) was added dropwise and when addition was complete the mixture was heated at reflux for 30 minutes. The reaction mixture was cooled on an ice-bath and saturated ammonium chloride (35 ml) was carefully added. The mixture was diluted with water (50 ml) and extracted with diethyl ether (2×50 ml). The combined organic extracts were washed with water, dried (Na2SO4) and the solvent was evaporated in vacuo to give 8.6 g of crude 5-cyclopropyl-5H-dibenzo[a,d]cyclohepten-5-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05595989 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-4850ab2726cd4a8db7991140b840ee6a |
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| Source note | uspto-grants-1997_01 |
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