HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620278Generated: October 30, 2026
1-Acetoxy-2-bromoethane → HCID 14372575, compound
https://huagongshe.com/reaction/620278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Acetoxy-2-bromoethane | HCID 13564 | — |
| Reactant | o-Desmethyl metoclopramide | HCID 9817332 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 14372575 | HCID 14372575 | 85.5% |
Reaction Steps
A solution of the tetrabutylammonium salt of 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide (5.27 g, 10 mmoles) (prepared in Preparation No. 3) in acetonitrile (100 ml) and 2-bromoethylacetate (2 g, 12 mmoles) was stirred for 48 hours. The solvent was evaporated and the residue partitioned between ethyl acetate and water. The organic layer was washed with ice-cold 0.4N sodium hydroxide solution, water, dried and the solvent evaporated. The residue was chromatographed over deactivated silica using methylene chloride (100 ), methanol (2), ammonia (0.5) solvent system. The appropriate fractions were combined and the solvent evaporated to leave a residue of 3.18 g (85%) of the title compound. Crystallization from toluene gave a sample, mp. 101°-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820715 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-eec40a5104f54b0dbe9ac58825ade751 |
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| Source note | uspto-grants-1989_04 |
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