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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020325Generated: November 2, 2026

Acetic Acid → HCID 58598873, compound

https://huagongshe.com/reaction/1020325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantChlorosuccinimideHCID 31398—
ReactantN-Ethylcarbamate 5-methoxy-8-methyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrroleHCID 86602843—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
ProductHCID 58598873HCID 585988737.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

N-chlorosuccinimide (0.39 g, 2.9 mmol) and acetic acid (3 mL) were added to a solution of N-ethylcarbamate-5-methoxy-8-methyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrrole (from Example 2, Step A) (0.80 g, 2.9 mmol) in DCE (3 mL). The resulting solution was stirred for 3 hours at 60° C. The reaction mixture was cooled to room temperature, diluted with CH2Cl2 (50 mL), and washed with H2O (50 mL). The organic extract was dried over MgSO4 and concentrated. The crude product was purified by column chromatography (SiO2) using a 0-35% EtOAc-hexanes gradient to afford 50 mg (6%) of the subtitle compound (The major product is N-ethylcarbamate-5-methoxy-6-chloro-8-methyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrrole, 78%). MS calculated for C16H20ClNO3+H: 310, observed: 310.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716324B2
Source datasetuspto-grants-2014_05
ORD IDord-59ace1f1222a49acb790aab65ca1104b
Source noteuspto-grants-2014_05