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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168586Generated: October 27, 2026

Isopropanol → Isopropyl-N,N,N',N'-tetraisopropylphosphorodiamidite

https://huagongshe.com/reaction/2168586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantTriethylamineHCID 8471—
ReactantBis(diisopropylamino)chlorophosphineHCID 2733425—
SolventDiethyl EtherHCID 3283—
ProductIsopropyl-N,N,N',N'-tetraisopropylphosphorodiamiditeHCID 53305816—

Reaction Conditions

Temperature0 °C

Reaction Steps

Bis(diisopropylamino)chlorophosphine (19, 250.1 g, 937 mmol) was dissolved in anhydrous ethyl ether (3.6 L) and triethylamine (190 g, 1.87 mol) was introduced. The turbid mixture was cooled at 0° C. and a solution of 2-propanol (225 g, 287 mL) in ether (200 mL) was added via a funnel. The resulting cloudy mixture was stirred at room temperature for 5.5 hours. The reaction was complete by checking with 31P NMR (δ=116.10 ppm, S). White solid (triethylamine HCl salt) was removed by filtration. The filtrate was concentrated to furnish a pale brown liquid (272 g, quantitative) and used for next step without further purification. Note that the P(III)-reagent can be purified by vacuum distillation (bp 84-86° C., 5 mm Hg) if desired to furnish a colorless clear oil. 1H NMR (CDCl3): δ 3.91 (m, 1H), 3.51 (m, 4H), 1.19 (d, 6H, J=6 Hz), 1.16 (24H, m). 31P NMR (CDCl3): δ 116.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045520B2
Source datasetuspto-grants-2015_06
ORD IDord-66f28ccdc0334eb5bfe58de4bd3dff4e
Source noteuspto-grants-2015_06