Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225050Generated: October 30, 2026

1-bromo-3-ethoxypropane → 5-(3-Ethoxypropyl)-3-iodo-5H-dibenzo[a,d]cyclohepten-5-ol

https://huagongshe.com/reaction/225050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-bromo-3-ethoxypropaneHCID 260493—
Reactant3-iodo-5H-dibenzo[a,d]cyclohepten-5-oneHCID 20232205—
SolventTetrahydrofuranHCID 8028—
Product5-(3-Ethoxypropyl)-3-iodo-5H-dibenzo[a,d]cyclohepten-5-olHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235820
Source datasetuspto-grants-1980_11
ORD IDord-6e426573da884e4b95107a3bac12fab8
Source noteuspto-grants-1980_11