HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-bromo-3-ethoxypropane → 5-(3-Ethoxypropyl)-3-iodo-5H-dibenzo[a,d]cyclohepten-5-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-bromo-3-ethoxypropane | HCID 260493 | — |
| Reactant | 3-iodo-5H-dibenzo[a,d]cyclohepten-5-one | HCID 20232205 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(3-Ethoxypropyl)-3-iodo-5H-dibenzo[a,d]cyclohepten-5-ol | HCID 23328870 | — |
Reaction Steps
3-Ethoxypropyl bromide (7.5 g., 0.045 mole) is converted to the Grignard reagent using standard procedures (see above). To this solution (ca 60 ml.), stirred in an ice bath, is added dropwise a solution of 10 g. (0.030 mole) of 3-iodo-5H-dibenzo[a,d]cyclohepten-5-one in 30 ml. of dry THF. The mixture is stirred for 5 minutes and concentrated in vacuo. The residue is treated with saturated ammonium chloride solution and extracted three times with ether. The ether layer is washed once with water, dried over sodium sulfate, and evaporated in vacuo to an orange solid, m.p. 95°-105° (12.0 g., 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04235820 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-6e426573da884e4b95107a3bac12fab8 |
| Source note | uspto-grants-1980_11 |