HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579548Generated: October 30, 2026
Triphenylphosphine → HCID 86663729, compound
https://huagongshe.com/reaction/579548
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | HCID 66833735 | HCID 66833735 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86663729 | HCID 86663729 | 70% |
Reaction Steps
A solution of tert-butyl 2-(tert-butoxycarbonyl(methyl)amino)-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butyl)hex-5-enoate (1.10 g, 2.29 mmol) in dichloromethane (30 mL) was cooled to −78° C. and treated with ozone until a pale blue-gray color appeared. After TLC indicated the absence of starting material, the ozone inlet tube was replaced with nitrogen and nitrogen was bubbled through the solution for 20 min to remove any excess ozone. Triphenylphosphine (1.50 g, 5.72 mmol, 2.5 equiv) was added in one portion, the cooling bath was removed and the mixture was stirred for 4 h. The solution was concentrated and purified by MPLC (0-40% ethyl acetate in heptane) gave tert-butyl 2-(tert-butoxycarbonyl(methyl)amino)-2-(3-oxopropyl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoate as a colorless oil (780 mg, 70%). Rf 0.40 (30% ethyl acetate in heptane). ESI MS found for C25H46BNO7 m/z [484.3 (M+1)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040703B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-b196ebd750754dddb5239e735de574b3 |
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| Source note | uspto-grants-2015_05 |
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