HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836770Generated: October 29, 2026
4-Chlorobutyryl chloride → HCID 12051895, compound
https://huagongshe.com/reaction/1836770
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | N-Methoxy-N-methyl-2-phenyl-isobutyramide | HCID 59788661 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12051895 | HCID 12051895 | 63% |
Reaction Steps
Slurry AlCl3 (10.15 g, 76.1 mmol) and methylene chloride (45 mL) under a nitrogen atmosphere at room temperature. Add 4-chlorobutyryl chloride (4.27 mL, 38.1 mmol), stir for minutes and add, by dropwise addition over 10 minutes, a solution of 2-methyl-2-phenyl-propionic acid, N-methoxy-N-methylamide (6.58 g, 31.7 mmol) in methylene chloride (15 mL). Stir at room temperature for 45 minutes, then heat at 30-35° C. for 7 hours. Pour into ice water (150 mL) and separate the layers. Wash the aqueous layer with water (3×75 mL), combine the aqueous layers and extract with methylene chloride (2×75 mL). Combine the organic layers and dry (Na2SO4). Filter, evaporate the filtrate in vacuo and purify by silica gel chromatography (3:1 hexane/ethyl acetate) give the title compound (6.19 g, 63%) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06777555B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-5f8b56fd19ee4567a6b82d60213818d6 |
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| Source note | uspto-grants-2004_08 |
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