HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromopropionic acid → (2-Carboxyethyl)triphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromopropionic acid | HCID 11553 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (2-Carboxyethyl)triphenylphosphonium bromide | HCID 2733850 | — |
Reaction Steps
A solution of 90 g. of triphenylphosphine and 50 g. of 3-bromopropionic acid in 550 ml. of acetonitrile was refluxed for two days. The reaction mixture was then distilled under reduced pressure to remove acetonitrile, and the residue was stirred well together with diethyl ether, and then the upper ethereal layer remoVed by decantation. The operation was repeated twice to form the crystalline product, which was recrystallised from acetonitriles, yield of the title compound: 115 g, m.p. 195°-198° C. Infra-red (hereinafter abbreviated to IR) absorption spectrum (potassium bromide tablet) 2880, 1740, 1434, 1382, 1322, 1230, 1105, 745, 690, 520 and 505 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04052512 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-6365c5f416264f769497a233432beb27 |
| Source note | uspto-grants-1977_10 |