HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Chlorophenyl)acetic acid → 6-Chloro-2-(4-chlorophenyl)hexanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Chlorophenyl)acetic acid | HCID 15880 | — |
| Reactant | 1-Chloro-4-iodobutane | HCID 82527 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Product | 6-Chloro-2-(4-chlorophenyl)hexanoic acid | HCID 58110109 | 90.7% |
Reaction Steps
Step AH (1): 2-(4-Chlorophenyl)acetic acid (2.5 g, 14.65 mmol) was deprotonated with NaHMDS (1.0 M in THF, 29.3 mL, 29.3 mmol) and reacted with 1-chloro-4-iodobutane (1.80 mL, 14.7 mmol) using a procedure analogous to Step AC (1) to afford 6-chloro-2-(4-chlorophenyl)hexanoic acid (3.47 g, 59% yield). LC-MS (M−H)− 259.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349880B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-d30373d31e294df88d4716266f7eee27 |
| Source note | uspto-grants-2013_01 |