HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165079Generated: October 31, 2026
Phosphorus tribromide → HCID 23043711, compound
https://huagongshe.com/reaction/2165079
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Methoxy-1-benzothiophene-2-carbaldehyde | HCID 12425910 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23043711 | HCID 23043711 | — |
Reaction Steps
To a solution of 3-methoxybenzothiophene-2-carboxaldehyde [3.4 g; J. Chem. Soc. C 779 (1967)] in ethanol (60 ml) was added sodium borohydride (0.34 g). After 10 minutes the solution was poured onto water (200 ml) and extracted with ether (2×50 ml). The ether extracts were washed with water (2×25 ml), dried and then evaporated to the title product as an orange oil. Yield, 3.4 g. 'HNMR (CDCl3, 60 MHz): 2.6 (s, 1H), 3.8 (s, 3H), 4.8 (s, 2H), 7.0-8.0 (m, 4H). This material (1.5 g) was dissolved in ether (20 ml). To the solution cooled in an ice-bath was added phosphorous tribromide (0.7 ml). The mixture was let to stand for 1 hour. The reaction mixture was poured onto ice-water (50 ml) and the ether layer separated, collected, dried and evaporated to obtain the title product as a light yellow oil (yield, 1.4 g). 'HNMR CDCl3, 60 MHz): 4.0 (s, 3H), 5.0 (s, 2H), 7.2-7.8 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04939140 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-5f09bf94869544988a0a6a89f64edacf |
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| Source note | uspto-grants-1990_07 |
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