HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322227Generated: October 29, 2026
HCID 22646671, compound → HCID 22009952, compound
https://huagongshe.com/reaction/322227
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22646671 | HCID 22646671 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22009952 | HCID 22009952 | — |
Reaction Steps
A solution of 0.091 g of ethyl 2-(4-amino-3-bromophenyl)-2-methylpropionate in 0.32 mL of concentrated hydrochloric acid was stirred at −10 to −5° C. in an ice-acetone bath as a solution of 0.023 g of sodium nitrite in 0.20 mL of water was added dropwise over about 15 minutes. Stirring was continued at this temperature for an additional 30 minutes. Next, the supernatant was removed by syringe and added dropwise over 10 minutes to a solution of 0.36 g of stannous chloride dihydrate in 0.25 mL of concentrated hydrochloric acid stirred under nitrogen in an ice-acetone bath. The addition was carried out at such a rate that the internal temperature remained at about −5° C. A gummy material separated during the addition. After completion of the addition, strrring was continued at −10 to −5° C. for 1 hour. The mixture was then diluted with 60 mL ethyl acetate and washed with sodium carbonate. The organic layer was washed with water and brine then dried over magnesium sulfate. Concentration in vacuo gave the crude title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211224B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-316503bb37d74a9aad19bf2a5393fed4 |
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| Source note | uspto-grants-2001_04 |
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