HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Ethylpiperidine → HCID 13750004, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Ethylpiperidine | HCID 13007 | — |
| Reactant | N-carbobenzyloxyalanine | HCID 736104 | — |
| Reactant | HCID 131714433 | HCID 131714433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13750004 | HCID 13750004 | — |
Reaction Steps
14 ml of chloro-sec. butyl formate added at -10 degrees C. to a solution of 23 grams of benzyloxycarbonyl alanine in 200 ml of methylene chloride and 14 ml of N-ethyl piperidine, 20.7 g of a product having a melting point of 109 to 111 degrees C. was obtained by the procedure described in Example 1 by crystallization from 60 ml of ethyl acetate and 200 ml of petroleum ether [α]D20 8.7 degrees (c 0.3; dimethylformamide).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04554100 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-d843857b3ff44f0686875856d8546bbb |
| Source note | uspto-grants-1985_11 |