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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583726Generated: November 1, 2026

N-Ethylpiperidine → HCID 13750004, compound

https://huagongshe.com/reaction/1583726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-EthylpiperidineHCID 13007—
ReactantN-carbobenzyloxyalanineHCID 736104—
ReactantHCID 131714433HCID 131714433—
SolventDichloromethaneHCID 6344—
ProductHCID 13750004HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04554100
Source datasetuspto-grants-1985_11
ORD IDord-d843857b3ff44f0686875856d8546bbb
Source noteuspto-grants-1985_11