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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711839Generated: October 30, 2026

Dichloromethane → HCID 66966216, compound

https://huagongshe.com/reaction/1711839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66966846HCID 66966846—
SolventDiethyl EtherHCID 3283—
ProductHCID 66966216HCID 6696621688%

Reaction Steps

A solution of (S)-(E)-3-(10-oxo-2,3,4,9,10,10a-hexahydro-1H-3a,8,9-triaza-benzo[f]azulen-6-yl)acrylic acid tert-butyl ester (0.65 g, 1.97 mmol) in CH2Cl2 (7 mL) was treated with TFA (7 mL). After stirring at room temperature for 30 min, the clear tan solution was concentrated in vacuo. The resulting oil was treated with anhydrous dioxane (20 mL of a 4.0 M solution in dioxane, 80 mmol). The resulting mixture was sonicated for 5 min, stirred under N2 for 5 min and diluted with Et2O. The solid was isolated by filtration, suspended in Et2O, concentrated to dryness, and dried under vacuum overnight to give the title compound (0.60 g, 88%) as an off-white solid: MS (ESI) m/e 274 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790709B2
Source datasetuspto-grants-2010_09
ORD IDord-e5cc84bd66324002ae9afbab4d43840f
Source noteuspto-grants-2010_09