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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849763Generated: November 2, 2026

Ammonium Chloride → Tert-butyl 3-chloro-4-(3-hydroxycyclohexyl)benzoate

https://huagongshe.com/reaction/1849763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodiumHCID 5360545—
ReactantTert-butyl 3-chloro-4-(3-oxocyclohexyl)benzoateHCID 86703645—
SolventMethanolHCID 887—
ProductTert-butyl 3-chloro-4-(3-hydroxycyclohexyl)benzoateHCID 8670364653%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of tert-butyl 3-chloro-4-(3-oxocyclohexyl)benzoate in anhydrous methanol (50 mL) was added sodium borobydride (1.04 g, 27.40 mmol) at 0° C. The reaction mixture was stirred for 1 hour at 0° C., after which saturated ammonium chloride solution (10 mL) was added. All volatiles were evaporated under reduced pressure, and the residue was partitioned between ethyl acetate (200 mL) and water (20 mL). The organic phase was washed with brine (10 mL), dried over sodium sulfate, and filtered. Concentration under reduced pressure gave a residue which was purified by silica gel column chromatography using 0-40% ethyl acetate in hexanes as eluent to afford the title compound as colorless oil (2.24 g, 53%): 1H NMR (300 MHz, CDCl3) δ 7.94-7.92 (m, 1H), 7.84-7.79 (m, 1H), 7.32-7.27 (m, 1H), 3.85-3.69 (m, 1H), 3.16-3.03 (m, 1H), 2.19-2.04 (m, 2H), 1.96-1.77 (m, 2H), 1.63-1.18 (m, 14H); MS (ES+) m/z 255.2, 257.1 (M−55).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952169B2
Source datasetuspto-grants-2015_02
ORD IDord-d314e415009d49d2ba5b6c004fdc9f4a
Source noteuspto-grants-2015_02