HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160471Generated: November 3, 2026
1,2-Dimethoxyethane → HCID 59516436, compound
https://huagongshe.com/reaction/1160471
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Isopropyl 2,2,2-trichloroacetimidate | HCID 21469209 | — |
| Reactant | HCID 59516434 | HCID 59516434 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 59516436 | HCID 59516436 | 96% |
Reaction Steps
Methyl (2S)-3-(3-pivaloyloxyphenyl)-2-hydroxypropionate (11 kg), 2,2,2-trichloro-1-isopropoxyethanimine (20 kg, 98 mol), 1,2-dimethoxyethane (10 L), and heptane (44 L) were mixed and stirred, and the resultant solution was cooled to 7° C. Trifluoromethanesulfonic acid (2.36 kg, 15.7 mol) was added dropwise to the reaction mixture over a period of 36 minutes, followed by stirring the reaction mixture at 25° C. for 19 hours. The reaction mixture was cooled to 7° C., to which heptane (66 L) was then added. The reaction mixture was then stirred for 45 minutes, followed by filtering off a white crystal of trichloroacetoamide. Water (55 L) was added to the filtrate for separating. Then, the organic layer was washed with a 5% sodium bicarbonate aqueous solution (52 L) twice and with water (55 L), followed by vacuum concentration to obtain 12.1 kg of the title compound (yield: 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816405B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-db83bb331f4f4fd98f430baf279fe45c |
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| Source note | uspto-grants-2010_10 |
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