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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bis(diisopropylamino)chlorophosphine | HCID 2733425 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Isopropyl-N,N,N',N'-tetraisopropylphosphorodiamidite | HCID 53305816 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045520B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-66f28ccdc0334eb5bfe58de4bd3dff4e |
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| Source note | uspto-grants-2015_06 |
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