Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Product | HCID 15508715 | HCID 15508715 | — |
Reaction Steps
In a four-necked flask equipped with a stirrer and a reflux condenser were placed 50 g of a Zn-Cu couple and 90 ml of tetrahydrofuran, followed by slowly charging a solution of 53 ml of t-butyl bromoacetate and 36 ml of 5-norbornen-2-carboxyaldehyde in 180 ml of tetrahydrofuran. After completion of the charging, the solution was subjected to reflux at 70° C. for 2 hours and then, cooled to room temperature. The Zn-Cu couple was filtered off, after which the solution was washed and extracted with the same solvent and distilled under vacuum to give 39 g of 3-bicyclo[2,2,1]hept-5-en-2-yl-3-hydroxy-propionic acid t-butyl ester (BHP) monomer, represented by the following structural formula M-I. ##STR8##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06146810 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-4af3bd2286a544aabea49689c8f8cb77 |
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| Source note | uspto-grants-2000_11 |
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