HuagongsheHuagongshe Chemistry Print Report · For research reference only
t-Butyl 1-bromocyclopentanecarboxylate → 2-(1-t-Butoxycarbonylcyclopent-1-yloxyimino)-2-(fur-2-yl) acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | t-Butyl 1-bromocyclopentanecarboxylate | HCID 21329494 | — |
| Reactant | 2-(Fur-2-yl)-2-hydroxyiminoacetic acid | HCID 72732783 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(1-t-Butoxycarbonylcyclopent-1-yloxyimino)-2-(fur-2-yl) acetic acid | HCID 54499267 | — |
Reaction Steps
The dipotassium salt of 2-(fur-2-yl)-2-hydroxyiminoacetic acid (syn isomer) was generated under an atmosphere of dry nitrogen and alkylated with t-butyl 1-bromocyclopentanecarboxylate using the method of Preparation 2. The product was isolated by pouring into water, acidifying and extracting in the conventional manner, thereby yielding the title compound, m.p. 106.8°-107.3°; λmax (pH 6 buffer) 277.5 nm (ε 15,100); τ(d6 -DMSO) values include 8.03, 8.30 (m, cyclopentyl protons) and 8.63 (C(CH3)3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04020058 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-39678c37907f48738e5254881c023b88 |
| Source note | uspto-grants-1977_04 |