HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248783Generated: October 25, 2026
Dichloromethane → t-Butyl (triphenylphosphoranylidene)propionate
https://huagongshe.com/reaction/2248783
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | tert-Butyl 2-bromopropanoate | HCID 545327 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | t-Butyl (triphenylphosphoranylidene)propionate | HCID 10916149 | 80.3% |
Reaction Steps
The t-butyl (triphenylphosphoranylidene)propionate was prepared as follows: Triphenylphosphine (33 g), t-butyl 2-bromopropionate (22 g) and triethylamine (12.7 g) were dissolved in ethyl acetate (150 ml), and stirred and heated under reflux for 48 hr, under an atmosphere of nitrogen. Methylene chloride (300 ml) was added to the cooled solution: the mixture was thoroughly washed with sodium hydroxide solution (10% w/w, 300 ml), water (200 ml) and brine; and dried (MgSO4). The solvent was evaporated and the residual oil triturated with hexane (2x200 ml) to give t-butyl (triphenylphosphoranylidene)propionate (33 g, 67%) as a yellow powder; mp 144°-151° C.; partial NMR (250 MHz, CDCl3): 1.0(br signal, 9H, t-butyl), 1.55(d, J=14.4 Hz, 3H, CH3), 7.3-7.9(complex m, 15H, ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05041460 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-2fd676c621494c22be734f00bf75f18e |
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| Source note | uspto-grants-1991_08 |
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