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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395167Generated: November 3, 2026

Phthalimide → HCID 178444658, compound

https://huagongshe.com/reaction/2395167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 137329066HCID 137329066—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178444658HCID 17844465873.1%

Reaction Steps

0.68 ml (4.36 mmol) of diethyl azodicarboxylate was slowly added dropwise under argon and while cooling with ice to a solution of 1.95 g (3.35 mmol) of [6-(tert-butyl-diphenyl-silanyloxymethyl)-10-hexyl-phenothiazin-4-yl]-methanol, 876 mg (5.03 mmol) of phthalimide and 968 mg (3.69 mmol) of triphenylphosphine in 25 ml of tetrahydrofuran. The reaction mixture was stirred at 0° for 2 hours and at room temperature for 20 minutes and then worked up analogously to that described in Example 2.1.1 ea. The residue was chromatographed on 250 g of silica gel with diethyl ether/hexane (1:3), whereupon, after precipitation from hexane, 1.74 g (73.1%) of 2-[6-(tert-butyl-diphenyl-silanyloxymethyl)-10-hexyl-phenothiazin-4-ylmethyl]-2,3-dihydro-1H-isoindole-1,3-dione were obtained as a light yellowish amorphous solid. MS: 710 (M+, 100), 653(61), 506(16), 370(36), 308(41), 268(40), 224(21), 160(34), 130(45), 43(43).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811548
Source datasetuspto-grants-1998_09
ORD IDord-95bcf63445e24d53984c0e04aa8f6cf6
Source noteuspto-grants-1998_09