HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → HCID 178525220, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | HCID 45156304 | HCID 45156304 | — |
| Product | HCID 178525220 | HCID 178525220 | — |
Reaction Steps
In a manner analogous to that described in Example 1, by the reaction of hydroxylamine with 1,1-cycloheptane-diacetic anhydride, there was obtained 1,1-cycloheptane-diacetic acid N-hydroxylimide (m.p. 90°-100° C.) which, by acylation with benzene-sulphonyl chloride, was converted into benzene-sulphonyloxy-1,1-cycloheptane, diacetic acid imide (m.p. 130°-133° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04152326 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-b4a4c72806a241f591105f47bf5a1e1a |
| Source note | uspto-grants-1979_05 |