HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 14552383, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 86746007 | HCID 86746007 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14552383 | HCID 14552383 | 99.9% |
Reaction Steps
Ethyl 8-(phenylmethyl)amino]-1,4-dioxaspiro -[4.5]-dec-7-ene-7-carboxylate (395.4 g, 1.3 mole) and acetic acid (75.0 ml, 1.3 mole) were added to ethanol (4 1). Sodium cyanoborohydride (82.0 g, 1. mole) was added in portions over 3 hours. The mixture was stirred overnight, then poured into water. The pH was adjusted to 10, and the product was extracted with methylene chloride, which was then dried with sodium sulfate and evaporated to give a yellow oil having small clear lumps in it. This was dissolved in THF and poured through 3 inches of basic alumina, which was then rinsed well with THF. The filtrate was evaporated to give 397.2 g (99.9%) of the title product as a yellow-green oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05134143 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-c789352fc66546fab2e5b536659d8a91 |
| Source note | uspto-grants-1992_07 |