HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423949Generated: October 28, 2026
Acetyl chloride → HCID 66673333, compound
https://huagongshe.com/reaction/423949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | trans-(7-Carbamoyl-1,1-diethyl-3-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)-carbamic acid tert-butyl ester | HCID 66673985 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66673333 | HCID 66673333 | 112.9% |
Reaction Steps
Acetyl chloride (278.8 mL, 3920 mmol) was added dropwise to ethanol (382 mL, 6530 mmol) at −5° C. over 2 h keeping the internal temperature below 20° C. The resulting solution was added portion wise over 15 min, keeping the internal temperature below 30° C., to a slurry of trans-(7-carbamoyl-1,1-diethyl-3-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-carbamic acid tert-butyl ester (123.0 g, 327 mmol) and ethanol (500 mL) that had been cooled to 10° C. The reaction mixture was stirred at room temperature for 2 h, and concentrated to ˜200 mL by rotary evaporation. Ethyl acetate (200 mL) was added and the resulting slurry was stirred at 0° C. for 30 min, filtered and dried to yield the hydrochloride salt of the title compound (102 g, >98% purity) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101794B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-b1dfea6092ec49c89f1c8e0dbc5fbf94 |
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| Source note | uspto-grants-2012_01 |
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