HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003170Generated: October 30, 2026
Chlorotrimethylsilane → HCID 18403062, compound
https://huagongshe.com/reaction/1003170
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dibenzyl 2-methylenepentanedioate | HCID 10947302 | — |
| Reactant | HCID 178520629 | HCID 178520629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18403062 | HCID 18403062 | 28% |
Reaction Steps
Benzyl[2,4-di(benzyloxycarbonyl)butyl]phosphinic acid Benzylphosphinic acid (2.3 g, 15 mmol) in 150 mL of dry dichloromethane was cooled to 0° C. under a nitrogen atmosphere. Triethylamine (6.5 g, 65 mmol) was added followed by trimethylsilyl chloride (5.8 g, 54 mmol) while the reaction temperature was maintained at 0° C. After 30 minutes dibenzyl 2-methylenepentanediote (2) in 20 mL of dichloromethane was added over 5 minutes. The reaction mixture was left to warm to room temperature and stirred overnight. The clear solution was cooled to 0° C. and quenched with 5% hydrochloric acid and with brine, dried (MgSO4) and evaporated to give a clear yellow liquid. Purification by flash chromatography and elution with 1:1 hexane/ethyl acetate containing 10% acetic acid yielded 2.0 g (28%) of benzyl[2,4-di(benzyloxycarbonyl)butyl]phosphinic acid (3, R=CH2Ph, R1+H) as a clear light yellow oil. Rf 0.37 (1:1 Hex./EtOAc, 10% AcOH). 1H NMR (d6-DMSO): 7.2 ppm(m,15H), 5.0 ppm(s,4H),3.0 (d,2H),2.8 ppm(m,lH),2.3 ppm(t,2H), 1.9 ppm(m,2H), 1.7 ppm(t,1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06046180 |
|---|
| Source dataset | uspto-grants-2000_04 |
|---|
| ORD ID | ord-691fe26bb7674a24a9cb1c4db00ecc15 |
|---|
| Source note | uspto-grants-2000_04 |
|---|