HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730425Generated: November 2, 2026
3-Iodo-2-methylprop-1-ene → HCID 54418976, compound
https://huagongshe.com/reaction/1730425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Iodo-2-methylprop-1-ene | HCID 10877752 | — |
| Reactant | HCID 54216006 | HCID 54216006 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Lithium Hydroxide | HCID 3939 | — |
| Product | HCID 54418976 | HCID 54418976 | — |
Reaction Steps
The starting material is prepared as follows: To the solution of 3.81 g of 4-(4-acetamidophenylmercapto)-3-amino-5-sulfamoylbenzoic acid in 25 ml of water and about 2 ml of 4 N aqueous lithium hydroxide (to adjust the pH to7.2), the solution of 2 g of 2-methylallyliodide in 2 ml of ethanol is added at room temperature while stirring and maintaining the pH between 6.7 and 7.0 with lithium hydroxide, and diluting the mixture with 10 ml ofethanol. After 23 hours (and the consumption of about 65% of the theoretical amount of lithium hydroxide) the mixture is washed with diethyl ether and acidified with hydrochloric acid. The precipitate formedis filtered off and recrystallized from aqueous ethanol, to yield the 4-(4-acetamidophenylmercapto)-3-(2-methylallylamino)-5-sulfamoylbenzoic acid melting at 193°-195°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03992440 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-c909106e3c9a426c9a373e0ac12c008c |
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| Source note | uspto-grants-1976_11 |
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