HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461998Generated: October 29, 2026
Bromochloromethane → Hexanedioic acid, chloromethyl phenylmethyl ester
https://huagongshe.com/reaction/1461998
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromochloromethane | HCID 6333 | — |
| Reactant | Benzyl adipate | HCID 19019622 | — |
| Product | Hexanedioic acid, chloromethyl phenylmethyl ester | HCID 10731820 | 48% |
Reaction Steps
To 350 ml of bromochloromethane cooled to 0° C. is added 67 g (0.14 mole) tetrabutylammonium salt of benzyl adipate half ester and the mixture is stirred overnight at 0° C. then allowed to warm to room temperature. The excess bromochloromethane is evaporated in vacuo, 400 ml ethyl ether is added to the residue and the mixture is stirred to form crystals of tetrabutylammonium bromide. The crystals are removed by filtration, washed with ether, stirred with ethyl acetate (300 ml) for one hour and refiltered and washed with ethyl acetate. The combined filtrates are evaporated in vacuo, the residue purified by chromatography on silica gel (1 kg), eluting with 2:1 hexane/ethyl acetate, to yield 19.1 g (48%) of the title compound. 1H-NMR (CDCl3) ppm (delta): 1.58-1.9 (m, 4H), 2.2-2.62 (n, 4H), 5.13 (s, 2H), 5.68 (s, 2H), 7.38 (s, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04457924 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-4c18d4f8cfac4018bcd935804ef4c60e |
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| Source note | uspto-grants-1984_07 |
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