HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 86737516, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 86737518 | HCID 86737518 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86737516 | HCID 86737516 | — |
Reaction Steps
Using the procedure of U.S. Pat. No. 2,775,597, the product of Step A4 was reacted with a solution of 15% hydrogen bromide in acetic acid for 2 hours at room temperature and the mixture was evaporated to dryness under reduced pressure to obtain dextrorotary trans 3-bromo-1-(3-methoxy-2-piperidyl)-2-propanone hydrobromide melting at 143° C. and having a specific rotation [α]D20 =+25° (c=1% in methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04252947 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-f85d5ccdaeb14e68957f8cdb650d8f13 |
| Source note | uspto-grants-1981_02 |