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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922609Generated: October 26, 2026

Methyl 5-(2-(tert-butoxycarbonylamino)acetamido)-2-hydroxybenzoate → Methyl 5-(2-aminoacetamido)-2-hydroxybenzoate

https://huagongshe.com/reaction/1922609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-(2-(tert-butoxycarbonylamino)acetamido)-2-hydroxybenzoateHCID 67174569—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 5-(2-aminoacetamido)-2-hydroxybenzoateHCID 59193335—

Reaction Steps

The methyl 5-(2-(tert-butoxycarbonylamino)acetamido)-2-hydroxybenzoate (1.3 g, 4.0 mmol) was dissolved in CH2Cl2 (15 mL) and TFA (8 mL). The reaction was stirred (RT, 2.5 h) and then concentrated to afford methyl 5-(2-aminoacetamido)-2-hydroxybenzoate as a clear oil. [M+H]+=225.1. The oil was dissolved in CH2Cl2 (20 mL) and to this was added DHA (1.3 g, 4.0 mmol), EDCl (0.84 g, 4.4 mmol) and triethylamine (2.0 g, 20.0 mmol). The reaction was stirred (RT, 4 h) and then partitioned between CH2Cl2 and brine. The aqueous layer was extracted with CH2Cl2, and the combined organic layers were dried over MgSO4. The crude material was purified by silica chromatography (0-5% MeOH/CH2Cl2) to afford 0.9 g of methyl 5-(2-(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamidoacetamido)-2-hydroxybenzoate as a tan solid. Mass calculated for C10H12N2O4=534.69; found: [M+H]+=535.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173831B2
Source datasetuspto-grants-2012_05
ORD IDord-5d3a0ac86b9743bc82a39faeca08ffcd
Source noteuspto-grants-2012_05