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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169110Generated: October 31, 2026

Hydrochloric Acid → 1-tert-Butyl 18-(2,5-dioxopyrrolidin-1-yl) octadecanedioate

https://huagongshe.com/reaction/2169110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborateHCID 9857522—
Reactant18-(Tert-butoxy)-18-oxooctadecanoic acidHCID 27282473—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Product1-tert-Butyl 18-(2,5-dioxopyrrolidin-1-yl) octadecanedioateHCID 58249213—

Reaction Steps

Octadecanedioic acid mono-tert-butyl ester (4.2 g, 0.011 mol) was dissolved in THF (20 mL), TSTU (4 g, 0.013 mol) in acetonitrile (20 mL) was added and pH of the solution was adjusted to 8 with dropwise addition of DIPEA. The mixture was stirred at RT for 4 h, then acidified with HCl (2M) to pH 3 and evaporated in vacuo. The residual oil was subsequently partitioned between ethyl acetate and HCl (0.1 M). The organic layer was dried (MgSO4), filtered and evaporated to dryness in vacuo. This afforded 5.2 g of octadecanedioic acid tert-butyl ester 2,5-dioxopyrrolidin-1-yl ester as an oil, which could be used in the next step without further purification. LC-MS (electrospray): m/z=468 (M+1) and 412 (M+1-tBu).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045560B2
Source datasetuspto-grants-2015_06
ORD IDord-24435b4a52ee480f8041c06c932f1dba
Source noteuspto-grants-2015_06