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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244792Generated: October 28, 2026

(R)-1-(3-Amino-4-benzyloxy-phenyl)-2-[benzyl-(5,6-diethyl-indan-2-yl)-amino]-ethanol → Acetic Acid (R)-1-(3-amino-4-benzyloxy-phenyl)-2-[benzyl-(2-methyl-indan-2-yl)-amino]-ethyl Ester

https://huagongshe.com/reaction/244792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-1-(3-Amino-4-benzyloxy-phenyl)-2-[benzyl-(5,6-diethyl-indan-2-yl)-amino]-ethanolHCID 53799063—
ReactantHCID 54033323HCID 54033323—
ProductAcetic Acid (R)-1-(3-amino-4-benzyloxy-phenyl)-2-[benzyl-(2-methyl-indan-2-yl)-amino]-ethyl EsterHCID 66823015—

Reaction Steps

The title compound is prepared from acetic acid (R)-2-[benzyl-(2-methyl-indan-2-yl)-amino]-1-(4-benzyloxy-3-nitro-phenyl)-ethyl ester (2.90 g) by an analogous procedure to that used to prepare (R)-1-(3-amino-4-benzyloxy-phenyl)-2-[benzyl-(5,6-diethyl-indan-2-yl)-amino]-ethanol in Example 19. The reaction is shown to be complete by TLC after 6 hours. The catalyst is filtered off and the solvent is removed in vacuo. The product is not purified further. TLC (silica, n-hexane/ethyl acetate 2:1 Rf=0.60).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658673B2
Source datasetuspto-grants-2014_02
ORD IDord-5c00e0ca80dc44929b98d4644d6e5c1b
Source noteuspto-grants-2014_02