HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381274Generated: November 5, 2026
1-(4-Amino-3,5-dichlorophenyl)-2-bromoethan-1-one → HCID 70451844, compound
https://huagongshe.com/reaction/1381274
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Amino-3,5-dichlorophenyl)-2-bromoethan-1-one | HCID 3015897 | — |
| Reactant | HCID 54361161 | HCID 54361161 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 70451844 | HCID 70451844 | — |
Reaction Steps
A mixture of 13.6 g of 4-amino-3,5-dichlorophenacyl bromide and 4.6 g of (R)-1-methyl-3-(4-aminocarbonylphenyl)propylamine in 100 ml of chloroform was warmed to 50° for 3 hours. The mixture was evaporated in vacuo, the residue was dissolved in 200 ml of methanol was 70 ml of water and a solution of 3.0 g of sodium borohydride in 20 ml of water was added dropwise thereto while cooling with ice and stirring so that the temperature did not rise above 20°. After completion of the addition, the mixture was stirred at 5°-10° for a further 2 hours, then poured into ice-water and extracted with methylene chloride. The material isolated from the methylene chloride extract was chromatographed on silica gel. With chloroform/n-propanol/25% ammonia (1000:10:1) there was obtained pure p-[(R)-3-[bis-[(RS)-4-amino-3,5-dichloro-β-hydroxyphenethyl]amino]butyl]benzamide in amorphous form; [α]D20 =-46° (c=1.0% in methanol); ε242 =31080; ε302 =7250.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04585796 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-5c40968b670c42a584a7584dc359db0e |
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| Source note | uspto-grants-1986_04 |
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