HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470543Generated: October 30, 2026
Tetrahydrofuran → Ethyl trans-4-Bromocinnamate
https://huagongshe.com/reaction/1470543
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | Ethyl trans-4-Bromocinnamate | HCID 688115 | 72% |
Reaction Steps
A solution of triethyl phosphonoacetate (13.1 g, 0.0589 mol) was added slowly (dropwise) to a solution of Potassium-tert-butoxide (6.59 g, 0.0589 mol), in dry THF (150 mL) at −5° C., stirred for 30-45 mins at the same temperature, then a solution of 4-Bromo benzaldehyde (10 g, 0.054 mol), in dry THF (50 mL) was slowly added dropwise at −5° C. over a period of 15 mins, stirred the reaction mixture for 30 mins at the same temperature. After completion of reaction by TLC, the reaction mixture was poured into ice water (300 mL), extracted with EtOAc (2×200 mL). The combined organic extracts were washed with sat NaHCO3 solution (200 mL), water (200 mL), brine (200 mL) and dried over anhydrous Na2SO4, filtered and evaporated to get crude (E)-ethyl 3-(4-bromophenyl)acrylate (10 g, 72%) as pale green liquid. This is carried to next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006449B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-1be8ea45632c4145a70f84f615b51d27 |
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| Source note | uspto-grants-2015_04 |
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