Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 20025664 | HCID 20025664 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14555673 | HCID 14555673 | — |
Reaction Steps
To a cold stirring suspension of 1 gm hydroxylamine hydrochloride and 1.3 gm sodium carbonate in 25 ml CH2Cl2 was added dropwise 1.58 gms 9(4-methoxyphenyl)nonanoyl chloride over a period of 15 min. The mixture was then stirred in the cold for a further 45 min, then 1.5 ml H2O was added, the mixture was allowed to warm up to room temperature, and stirring was continued for 72 hrs. The precipitated solid was filtered, washed with water, and crystallized twice from CH2Cl2 to give A. The filtrate from the reaction mixture was evaporated in vacuo to give a granular solid which was also crystallized twice from CH2Cl2 to give B. A and B were shown to be the same by spectral comparison. Total yield (A+B)=1.58 gm (51%) m.p. 96°-98° C. Elemental analysis: calculated C 67.90, H 8.90, N 4.95. Found C 67.96, H 9.08, N 4.95 (calculated for 0.2 moles H2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04861798 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-9d714760a014484fa474acd54d904c79 |
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| Source note | uspto-grants-1989_08 |
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