HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979415Generated: October 29, 2026
N,N-Dimethylaniline → HCID 20200020, compound
https://huagongshe.com/reaction/979415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Ethyl 6-hydroxyhexanoate | HCID 357781 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20200020 | HCID 20200020 | 48.3% |
Reaction Steps
160 g of ethyl 6-hydroxy-hexanoate, 145.4 g of N,N-dimethylaniline and 200 ml of anhydrous toluene are placed in a round flask which is provided with a dropping funnel, a thermometer and a stirrer. 119.4 g of ethyl chloroformate are added dropwise at 25° C. within a half hour while stirring. The reaction mixture is held under reflux for 3 hours. After cooling the reaction mixture is poured on to ice-water, the organic phase is washed twice with water, with 100 ml of a 5% hydrochloric acid solution and then neutral with water. After drying over sodium sulphate the solvent is distilled off. 173 g of crude product are obtained. Fractional distillation gives 112 g (yield 48.3% of theory) of chemically pure ethyl 6-ethoxycarbonyloxy-hexanoate; 75 g thereof can be used as an olfactorily pure product without further treatment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04668433 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-81cf8ea596da49babe5b8a2cc6bdcf8a |
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| Source note | uspto-grants-1987_05 |
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