HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11074Generated: October 28, 2026
Lithium diisopropylamide → HCID 11843963, compound
https://huagongshe.com/reaction/11074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Phosphonium, [(2-bromophenyl)methyl]triphenyl-, bromide | HCID 11733967 | — |
| Reactant | 9-hydroxy-4-iodopyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione | HCID 11842834 | — |
| Product | HCID 11843963 | HCID 11843963 | — |
Reaction Steps
The 5-methoxy-1H-indole-2-carbaldehyde (1) was reacted with (2-bromobenzyl)(triphenyl)phosphonium bromide using the procedure described in example 37, except that the aldehyde was added at 0° C., the ratio of LDA:aldehyde was 1.46:1 and the reaction time was 5 h, to give (after crystallisation from CH2Cl2/hexane) the diene (531) as a yellow solid (the pure E isomer) (88%), mp 120–123° C. 1H NMR (CDCl3) δ 8.21 (br s, 1H), 7.66 (dd, J=7.9, 1.5 Hz, 1H), 7.59 (dd, J=8.1, 1.0 Hz, 1H), 7.32 (br t, J=7.1 Hz, 1H), 7.27 (d, J=8.3 Hz, 1H), 7.22 (d, J=16.4 Hz, 1H), 7.12 (td, J=7.6, 1.5 Hz, 1H), 7.05 (d, J=16.4 Hz, 1H), 7.04 (d, J=2.4 Hz, 1H), 6.88 (dd, J=8.8, 2.4 Hz, 1H), 6.59 (d, J=1.7 Hz, 1H), 3.86 (s, 3H). Found: C, 61.97; H, 4.30; N, 4.17. C17H14BrNO requires C, 62.21; H, 4.30; N, 4.27.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07094798B1 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-1db8bc6974f04497a060aa2801e1f53f |
|---|
| Source note | uspto-grants-2006_08 |
|---|