HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397590Generated: October 30, 2026
Hydrochloric Acid → HCID 70025612, compound
https://huagongshe.com/reaction/397590
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2-Chloroethyl)pyrrolidine hydrochloride | HCID 81668 | — |
| Reactant | HCID 12114663 | HCID 12114663 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 70025612 | HCID 70025612 | — |
Reaction Steps
A mixture of (4-methoxyphenyl)-(4-hydroxyphenyl)-1,2,3,4-tetrahydronaphth-1-yl-methane (400 mg, 0.001 mol), anhydrous K2CO3 (2.0 gm, 0.14 mol), 1-(2-chloroethyl)pyrrolidine hydrochloride (400 mg, 0.002) and dry acetone (25.0 ml) was refluxed for 10 hrs. K2CO3 was filtered off, acetone was distilled off and the residue was diluted with water. The reaction mixture was extracted with ethyl acetate, washed with water, dried over sodium sulphate and concentrated to give an oil which was filtered through basic alumina column using benzene as the eluent, and concentrated to give an oil. The oil thus obtained was treated with ethanolic HCl. The solvent was evaporated and the compound was crystallized with absolute alcohol and dry ether, filtered under anhydrous conditions, and dried to give the title compound of formula I. Yield 350 mg. (68.35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610705B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-7d0f94d9d3e44f81a8ebbee67c562b3f |
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| Source note | uspto-grants-2003_08 |
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