HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-5-[2-n-propyl-3-hydroxy-4-acetylphenoxy]-pentane → Diethyl 4-[[[5-(4-acetyl-3-hydroxy-2-propylphenoxy)pentyl]thio]methyl]-1,3-oxathiolane-2,2-dipropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-5-[2-n-propyl-3-hydroxy-4-acetylphenoxy]-pentane | HCID 13763298 | — |
| Reactant | Diethyl 4-(mercaptomethyl)-1,3-oxathiolane-2,2-dipropanoate | HCID 14405886 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Diethyl 4-[[[5-(4-acetyl-3-hydroxy-2-propylphenoxy)pentyl]thio]methyl]-1,3-oxathiolane-2,2-dipropanoate | HCID 14405889 | 93% |
Reaction Steps
The reaction of the mercaptan from Example 1 (2.0 g, 0.006 mol) and 5-(2-n-propyl-3-hydroxy-4-acetylphenoxy)-1-bromopentane (described in U.S. Pat. No. 4,565,882, Example 1) (2.1 g. 0.06 mol) in methyl ethyl ketone (20 ml) was carried out and worked up in the same manner as described in Example 2. After chromatography on silica gel using 25% ethyl acetate/hexane as eluent, 3.3 g (93%) of the title compound was obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808729 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-c4e4942c5ffb4d5ba20cae47951cb3dc |
| Source note | uspto-grants-1989_02 |