HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243641Generated: October 31, 2026
Diisopropylethylamine → HCID 178523333, compound
https://huagongshe.com/reaction/1243641
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Chlorophenyl chloroformate | HCID 139059 | — |
| Reactant | HCID 178511032 | HCID 178511032 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178523333 | HCID 178523333 | 59.1% |
Reaction Steps
0.205 g (0.60 mmol) of trans-3-[5-(6-cylcopropylmethoxynaphthalen-1-yl)-1,3-dioxan-2-yl]propylamine is added, in small portions and at ambient temperature, to a solution of 0.110 ml (0.78 mmol) of 4-chlorophenyl chloroformate and 0.205 ml (1.2 mmol) of N,N-diisopropylethylamine in 6 ml of dichloromethane. The mixture is stirred at ambient temperature for 16 hours, then washing is carried out with 5 ml of a saturated sodium bicarbonate solution. The phases are separated and the organic phase is filtered through a hydrophobic sintered glass funnel. The filtrate is concentrated under reduced pressure and the residue is purified by chromatography on silica gel, eluting with an 80/20 mixture of cyclohexane and ethyl acetate. After washing in 5 ml of diisopropyl ether, 0.176 g of a white solid is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119116B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-0c8c8d06ac8c4981af0233d96ac1ea80 |
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| Source note | uspto-grants-2006_10 |
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