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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1607745생성일: 2026년 10월 23일

Benzaldehyde → Methyl 2,6-bis(benzylideneamino)hexanoate

https://huagongshe.com/ko/reaction/1607745

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물Lysine hydrochloride, DL-HCID 12047—
반응물Methyl DL-lysinate dihydrochlorideHCID 13661416—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물Methyl 2,6-bis(benzylideneamino)hexanoateHCID 14231031—

반응 단계

A suspension of 2,6-diaminohexanoic acid hydrochloride (18.26 g, 100 mmol) in dry methanol (100 ml) is saturated with gaseous hydrochloric acid and heated under reflux for 2 hours. Upon cooling, methyl 2,5-diaminhexanoate dihydrochloride crystallizes. To an ice cooled suspension of methyl 2,6-diaminohexanoate dihydrochloride (4.66 g, 20 mmol) in methylene chloride (50 ml) is added benzaldehyde (4.04 g, 40 mmol) and then dropwise a solution of triethylamine (4.24 g, 40 mmol) in methylene chloride (30 ml). The reaction mixture is allowed to stand overnight at room temperature under stirring and is then concentrated under reduced pressure to give a residue which is extracted into ether (diethyl ether). The ether extract is washed with water and brine, dried over MgSO4, and concentrated to give methyl 2,6-bis(benzylideneamino)hexanoate as an oily residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04866206
출처 데이터셋uspto-grants-1989_09
ORD IDord-6cb7627b6c384bcc96650ac41c9eddf1
출처 메모uspto-grants-1989_09