HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864993Generated: October 30, 2026
Triphenylphosphine → HCID 19027593, compound
https://huagongshe.com/reaction/864993
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 54465974 | HCID 54465974 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19027593 | HCID 19027593 | 82.5% |
Reaction Steps
A solution of 4-acetoxy-2-hydroxymethylbutyl acetate (11.04 g, 0.054 mol) and triphenylphospine (21.27 g, 0.081 mol) in dry dichloro methane (150 ml) was stirred at 0° C., and N-bromo-succinimide (14.43 g, 0.081 mol) was added in portions. The mixture was kept at 0° C. for 20 h, evaporated to small volume and stirred with 50 ml of ethyl acetate+n-hexane (1+1). The white triphenylphospine oxide was filtered off and washed with a little ethyl acetate+n-hexane (1-1). The combined filtrate was evaporated and purified on a 200 g SiO2 column with ethyl acetate+n-hexane (1+1) as eluent. The 250-550 ml fraction was evaporated in vacuum to give 11.90 g (82%) of pure 4-acetoxy-2-bromomethylbutyl acetate. TLC on silica (ethyl acetate+n-hexane 1+1): Rf 0.59.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05565461 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-1280e15616b043448e175535910f100f |
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| Source note | uspto-grants-1996_10 |
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