HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Bromomethyl)-3-phenoxybenzene → 3-Phenoxybenzyl alpha-fluoro-alpha-isopropylphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Bromomethyl)-3-phenoxybenzene | HCID 94544 | — |
| Reactant | alpha-Fluoro-3-phenoxybenzyl alpha-isopropyl-4-chlorophenylacetate | HCID 20507332 | — |
| Reactant | alpha-Fluoro-alpha-isopropylphenylacetic acid | HCID 54262117 | — |
| Product | 3-Phenoxybenzyl alpha-fluoro-alpha-isopropylphenylacetate | HCID 54191148 | — |
Reaction Steps
This compound was prepared from 3-phenoxybenzyl bromide and α-fluoro-α-isopropylphenylacetic acid following the method used in Example 2 Method B for the preparation of α-fluoro-3-phenoxybenzyl α-isopropyl-4-chlorophenylacetate. The product, a colourless oil, was characterised by pmr spectroscopy. Chemical shift ppm (solvent CDCl3): 0.69(3H, d, J=6 Hz, CH3); 1.05 (3H, d of d, J=6 Hz and J=2 Hz, CH3); 2.34(1H, m, CH(CH3)2); 3.27 (1H, d, J=10 Hz, CH); 7.17(1H, d of d, J=56 Hz and J=2 Hz, CHF) and c. 7.20(14H, m, aromatic protons).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04376784 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-92b6fd9b7dee4459837ae2b55880cb16 |
| Source note | uspto-grants-1983_03 |