HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986408Generated: October 30, 2026
Ammonium Chloride → HCID 13537257, compound
https://huagongshe.com/reaction/986408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(Bromomethyl)-3-phenoxybenzene | HCID 94544 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 13537254 | HCID 13537254 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13537257 | HCID 13537257 | — |
Reaction Steps
A Grignard reagent prepared from 3-phenoxybenzyl bromide (0.98 g), magnesium turnings (0.1 g) in dry diethyl ether (15 ml) under an atmosphere of nitrogen, is cooled with vigorous stirring to -78° C. To this is added a solution of 1-(4-ethoxyphenyl)-1-(2-oxoethyl)-cyclopropane (0.5 g) in diethyl ether (15 ml) over 5 min. The resulting mixture is allowed to warm up to room temperature over 1 h. Saturated NH4Cl solution is added and the mixture extracted with diethyl ether (x3), dried and the solvent evaporated under reduced pressure. The product is purified by t.l.c. on silica eluted with 10% diethyl ether in petroleum ether (b.p. 60°-80° C.). Yield 0.25 g, nD 1.5444.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04713392 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-123436258846482aaf49c5f3d09bdbe0 |
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| Source note | uspto-grants-1987_12 |
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