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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678284Generated: November 1, 2026

Triphenylphosphine → HCID 66849850, compound

https://huagongshe.com/reaction/1678284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantN-(Triphenylmethyl)-L-serine methyl esterHCID 7128367—
ReactantN-Cbz4-(4-hydroxyphenyl)butylamineHCID 11637991—
SolventBenzeneHCID 241—
ProductHCID 66849850HCID 6684985064.7%

Reaction Steps

Commercially available N-trityl-L-serine methyl ester (1.60 g, 5.34 mmol) was combined with triphenylphosphine (1.28 g, 4.88 mmol) and [4-(4-hydroxyphenyl)butyl]carbamic acid benzyl ester (2.0 g, 6.68 mmol) in benzene (40 mL) at room temperature. Diisopropyl azodicarboxylate (0.958 mL, 4.86 mmol) was added dropwise and the reaction was stirred for 14 days. The solvent was removed under reduced pressure and the residue was purified by column chromatography (silica gel, eluent: 6:1, v/v dichloromethane/ethyl acetate) to provide compound 10 (2.22 g, 51%). 1H NMR (300 MHz, CDCl3) δ 7.52 (m, 6H), 7.39-7.14 (m, 14H), 7.06 (d, 2H), 6.79 (d, 2H), 5.09 (s, 2H), 4.72 (m, 1H), 4.24 (m, 1H), 4.01 (m, 1H), 3.72 (m, 1H), 3.22 (s, 3H), 3.18 (m, 2H), 2.88 (d, 1H), 2.57 (m, 2H), 1.66-1.48 (m, 4H). Rf=0.91 (5:1 v/v dichloromethane/ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008494B2
Source datasetuspto-grants-2011_08
ORD IDord-53d4b5e1e762410da925771d984c93f0
Source noteuspto-grants-2011_08