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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518753Generated: October 25, 2026

Diisopropylethylamine → HCID 178474991, compound

https://huagongshe.com/reaction/518753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Fluoro-4-nitrobenzyl alcoholHCID 2774658—
ReactantHCID 178474995HCID 178474995—
SolventAcetonitrileHCID 6342—
ProductHCID 178474991HCID 17847499117.24%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of N-(trans-4-aminocyclohexyl)acetamide hydrochloride (200 mg, 1.038 mmol) and DIPEA (0.494 mL, 2.83 mmol) in ACN (2 mL) was added (3-fluoro-4-nitrophenyl)methanol (161 mg, 0.944 mmol). The resulting mixture was stirred overnight at 80° C. After 16 hours, the reaction was concentrated and the residue purified by column chromatography, eluting with 0-10% MeOH in DCM, to provide N-(trans-4-(5-(hydroxymethyl)-2-nitrophenylamino)cyclohexyl)acetamide as a yellow powder (50 mg, 17.24% yield). MS, m/z (C15H21N3O4): calcd, 307.2. found, 308.1 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-4caa372f18fa4551af1b264dfbaf3456
Source noteuspto-grants-2015_08