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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971300Generated: November 1, 2026

Hydrochloric Acid → (2R,4R)-1-(tert-butoxycarbonyl)-4-(2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamido)piperidine-2-carboxylic Acid

https://huagongshe.com/reaction/1971300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
Reactant(2R,4R)-1-tert-butyl 2-methyl 4-(2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamido)piperidine-1,2-dicarboxylateHCID 67266415—
SolventMethanol tetrahydrofuran waterHCID 21892291—
Product(2R,4R)-1-(tert-butoxycarbonyl)-4-(2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamido)piperidine-2-carboxylic AcidHCID 6726631296.1%

Reaction Steps

LiOH (1.23 g, 51.4 mmol) was added to a solution of (2R,4R)-1-tert-butyl 2-methyl 4-(2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamido)piperidine-1,2-dicarboxylate (5.4 g, 12.8 mmol) in THF/MeOH/water (3:2:1) (60 mL) and the resulting solution was stirred at room temperature for 18 hours. 1M HCl solution was added to reaction solution to adjust pH to about 3, extracted with ethyl acetate (2×100 mL). The organic layers were dried over MgSO4 and concentrated to give the acid as a white solid 5.0 g (96%). LC-MS: 407.3; 405.3 (t=2.2 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431597B2
Source datasetuspto-grants-2013_04
ORD IDord-54462bc9e8e3407c805dfa76bfa0164d
Source noteuspto-grants-2013_04