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HRID 52819作成日:2026年10月24日

(1R,2S)-(+)-cis-1-Amino-2-indanol → Indene

https://huagongshe.com/ja/reaction/52819

反応式

関与物質

役割名称HCID仕込み量
反応物(1R,2S)-(+)-cis-1-Amino-2-indanolHCID 2725045—
反応物(1S,2R)-(-)-1-Amino-2-indanolHCID 9866743—
生成物IndeneHCID 7219—

反応手順

The trans amide can be made from the epoxide either (1) by treating the indene oxide with ammonia or a primary amine to produce a trans-1-amino-2-indanol and reacting the trans-1-amino-2-indanol with an acylating agent, or (2) by treating the epoxide with an amide anion to produce the trans hydroxy amide directly. In one embodiment the indene is oxidized with aqueous hypochlorite in the presence of a chiral salen catalyst to produce a partially resolved epoxide, which is converted to the partially resolved trans-1-amino-2-indanol by treating with ammonia or a primary amine followed by acylating with benzoyl chloride or acetic anhydride. The resulting benzamide or acetamide is recrystallized to yield substantially optically pure trans-1-benzamido-2-indanol or trans-1-acetamido-2-indanol. In two preferred embodiments, the cis-1-amino-2-indanols are (1S,2R)-1-amino-2-indanol and (1R,2S)-1-amino-2-indanol, produced by oxidation of indene in the presence of an R,R or S,S-salen catalyst respectively.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616808
出典データセットuspto-grants-1997_04
ORD IDord-03ac5c50e00d4380b377431b60ad5e1f
出典メモuspto-grants-1997_04