HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromohexane → 4-(Hexyloxy)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | 4-(Octyloxy)benzoic acid | HCID 17231 | — |
| Product | 4-(Hexyloxy)benzoic acid | HCID 70834 | — |
Reaction Steps
The same procedure as in the synthesis of 4-octyloxy benzoic acid of Example 26 was repeated except that bromohexane was used instead of bromooctane to obtain 4-hexyloxy benzoic acid. This 4-hexyloxy benzoic acid was condensed with (+)-4-(2-methyloctanoyl) phenol in the same manner as in the synthesis of 4-(2-methyloctanoyl) phenyl, 4-octyloxy benzoic acid ester of Example 26 to synthesize 4-(2-methyloctanoyl) phenyl, 4-hexyloxy benzoic acid ester having the aforementioned physical and chemical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05137653 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-f6610b4e843a46cfb17890cead96a842 |
| Source note | uspto-grants-1992_08 |