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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11074Generated: October 28, 2026

Lithium diisopropylamide → HCID 11843963, compound

https://huagongshe.com/reaction/11074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
ReactantPhosphonium, [(2-bromophenyl)methyl]triphenyl-, bromideHCID 11733967—
Reactant9-hydroxy-4-iodopyrrolo[3,4-c]carbazole-1,3(2H,6H)-dioneHCID 11842834—
ProductHCID 11843963HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094798B1
Source datasetuspto-grants-2006_08
ORD IDord-1db8bc6974f04497a060aa2801e1f53f
Source noteuspto-grants-2006_08